Methods of identifying gene expression products resultant from alternative splicing and methods of diagnosing and treating disorders associated therewith

ABSTRACT

A method of identifying latent splice sites, the method comprising identifying at least one intronic in-frame stop codon located upstream of a 5′ splice site sequence being a latent splice site, thereby identifying latent splice sites.

FIELD AND BACKGROUND OF THE INVENTION

The present invention relates to methods of identifying gene expression products which result from alternative splicing and more particularly to methods of diagnosing and treating disorders associated with the expression of such gene products, such as cancer.

Alternative splicing, the process by which multiple messenger RNA (mRNA) isoforms are generated from a single pre-mRNA species is an important means of regulating gene expression. Alternative splicing plays a central role in numerous biological processes such as sexual differentiation in Drosophila and apoptosis in mammals [Lopez (1998) Ann. Rev. Genet. 32:279-305]. Aberrant splicing generates abnormal mRNAs which are either unstable or code for defective or deleterious protein isoforms which are frequently implicated in the development of human disease [Lopez (1998) Ann. Rev. Genet. 32:279-305; Charlet (2002) Mol. Cell 10:45-53].

The significance of alternative splicing is further extended in the post genomic era. On the basis of the initial drafts of the human genome sequence it was estimated that 30,000-40,000 genes comprise the human genome [International Human Genome Sequencing Consortium. Nature 2001 409:860-921; Venter (2001) Science 291:1304-1351]. Although final gene counts may be higher, there is a disparity between the relatively small number of human genes and the complexity of the human proteome, suggesting that alternative splicing is important in the generation of protein diversity. The most striking example of alternative splicing complexity known, is the single pre-mRNA for a Drosophlia axon guidance receptor gene, Down Syndrome cell-adhesion molecule (Dscam), which can be processed to generate potentially 38,016 different mature transcripts [Schmucker (2000) Cell 101:671-684].

The accuracy and efficiency of the gene splicing reaction is attributed mainly to a number of cis sequence elements and trans-acting factors which are required for splicing.

Cis Sequence Elements

Any constitutive or alternative splicing event requires the assembly of the basal splicing machinery in spliceosome complexes on consensus sequences present at all boundaries between introns and exons, herein after the 5′ splice site (5′SS) and 3′ splice site (3′SS). The spliceosome has two functions; to recognize and select splice sites and to catalyze the two sequential transesterification reactions, which remove the introns and join the two exons together. The efficiency with which the splicosome acts on an exon is determined by a balance of several features, including the strength of a splice site essentially conformity to consensus splice site sequences, exon size and the presence of auxiliary cis elements. Exons of ideal size, (i.e., 50-300 nucleotides) with well conserved splice site sequences are recognized efficiently by the splicing machinery and are constitutively included in the transcript, whereas suboptimal exons require auxilliary elements for recognition. Typically, auxiliary elements which regulate the usage of alternative splice sites share several common features; they are small and variable in sequence and mostly present in multiple copies. Although most of these elements are single stranded, secondary structures have been implicated in the function of a few elements. Despite high level of conservation auxiliary cis elements are degenerate, rendering identification thereof difficult. Interestingly, auxiliary cis elements can be both exonic and intronic. Intronic cis elements can lie upstream, downstream or flanking both sides of the regulated exon and can be positioned proximally or distal to the regulated exon, however in most cases they are located close to the exon. Notably, such cis elements can enhance or repress splice site selection. Thus, depending on the location of the auxiliary cis elements and the effect thereof on the recognition of alternative splice sites, the elements are referred to as exonic splicing enhancers or silencers or intronic splicing enhancers or silencers. Ladd and Cooper list intronic splicing enhancers and silencers identified to date [(2002) Gen. Biol. 3(11):1-16]. Exonic splicing enhancers and silencers are described in Fairbrother (2002) Science 297:1007-1013

It is suggested that many alternative splice sites are associated with both enhancers and silencers and that regulation thereof is often the result of a dynamic antagonism between proteins binding such elements (i.e., trans-acting factors)

Trans-Acting Splicing Factors

The SR family of proteins—The SR proteins, a group of highly conserved proteins in metazones, are required for constitutive splicing and also affect alternative splicing regulation. They have a modular structure consisting of one or two copies of an RNA-recognition motif (RRM) and a C-terminal domain rich in alternating serine and arginine residues (the RS domain). The RRMs determine RNA binding specificity, whereas the RS domain mediates protein-protein interactions that are thought to be essential for the recruitment of the splicing apparatus and for splice-site pairing [Fu (1995) RNA 1:663-680; Graveley (2000) RNA 6:1197-1211; Tacke (1999) Curr. Opin. Cell. Biol. 11:358-362; Wu (1993) Cell 75:1061-1070].

Another class of RS domain containing proteins involved in splicing are the RS-related proteins (SRrps). These proteins which oftentimes contain RRMs, include the U1-70K protein, both subunits of U2AF, SRm 160/300 (two SR-related nuclear matrix proteins of 160 and 300 kDa), as well as alternative splicing regulators such as Tra and Tra2 [Pu (1995) RNA 1:663-680; Graveley (2000) RNA 6:1197-1211]. SR family and SR-related proteins function in the recognition of exonic splicing enhancers (ESEs) leading to the activation of suboptimal adjacent 3′ splice sites [Blenckowe (2000) Trends Biochem. Sci. 25:106-110].

Polypyrimidine tract binding proteins (PTB)—These RNA binding proteins, also termed hnRNPI, recognize the polypyrimidine tracts preceding 3′ splice sties and have a role as negative regulators of splicing. PTB repress several neuron specific exons in non-neuronal cells, as well as smooth muscle-specific inclusion of alternatively spliced exons in the a-tropomyosin and a-actinin pre-mRNAs. PTB and U2AF bind competitively to the polypyrimidine and this competitive binding has been proposed as the basis for the negative regulatory effects of PTB. However, more complex mechanisms of regulation by PTB are also likely to operate since binding of PTB to sites on both sides of the neuronal specific N1 exon in the mouse c-src pre-mRNA is required for repression [Valcarcel (1997) Curr. Biol. 7:R705-R708]

The CELF protein family—This family of proteins are involved in cell-specific and developmentally regulated alternative splicing [Ladd (2001) Mol. Cell. Biol. 21:1285-1296]. These RNA binding proteins contain three RRNs and divergent linker domain of unknown function. Several members of the family exhibit tissue specific expression and others are more broadly expressed. CELF proteins bind to muscle specific enhancers (MSE) in the cardiac Troponin-T gene (cTNT) and promote inclusion of the developmentally regulated exon 5.

Despite significant development of the splicing research, the ability to accurately predict splicing patterns is still difficult especially in light of the observation that functional splice sites do not always match the consensus sequences well, while many cryptic sites in the genome match the consensus but are not normally recognized by the splicing machinery. For example, a key step in pre-mRNA splicing involves the recognition and selection of a consensus sequence at the 5′ splice site (5′SS). Frequently, however, sequences which comply with the consensus are not selected for splicing [Green (1991) Annu. Rev. Biochem. 65:367-409]. These findings suggest that the sequence surrounding a splice site as well as the match thereof to the consensus, strongly affects the recognition of the splice site.

While reducing the present invention to practice the present inventors have uncovered that intronic in-frame stop codons located upstream to 5′SS sequence inactivate splicing from such splice sites. These findings enable to accurately and efficiently predict gene expression products in-silico.

SUMMARY OF THE INVENTION

According to one aspect of the present invention there is provided a method of identifying latent splice sites, the method comprising identifying at least one intronic in-frame stop codon located upstream of a 5′ splice site sequence being a latent splice site, thereby identifying latent splice sites.

According to another aspect of the present invention there is provided a method of identifying a putative pathogenic gene, the method comprising identifying an in-frame stop codon in an intronic sequence of the gene, thereby identifying the putative pathogenic gene.

According to yet another aspect of the present invention there is provided a computer readable storage medium comprising data stored in a retrievable manner, the data including a plurality of genes each having an in-frame stop codon in an intron thereof.

According to further features in preferred embodiments of the invention described below, the data is as set forth in Table 6.

According to still another aspect of the present invention there is provided a method of uncovering genes associated with a pathogenic tissue, the method comprising: (a) identifying genes having an in-frame stop codon in an intronic sequence thereof; and (b) detecting a presence or absence of a truncated expression product resultant of the in-frame stop codon in a gene of the genes which is expressed in the pathogenic tissue, thereby uncovering genes associated with the pathogenic tissue.

According to an additional aspect of the present invention there is provided an oligonucleotide useful for detecting abnormally spliced nucleic acid sequences, the oligonucleotide comprising a nucleic acid sequence specifically hybridizable with a polynucleotide sequence including at least one in-frame stop codon located in an intronic sequence of a gene.

According to still further features in the described preferred embodiments the gene is selected from the group consisting of the genes set forth in Table 6.

According to yet an additional aspect of the present invention there is provided a kit useful for detecting abnormally spliced nucleic acid sequences, the kit comprising at least one oligonucleotide including a nucleic acid sequence specifically hybridizable with a polynucleotide sequence including at least one in-frame stop codon located in an intronic sequence of a gene and reagents for detecting the at least one oligonucleotide when hybridized to the polynucleotide sequence.

According to still further features in the described preferred embodiments the at least one oligonucleotide is labeled.

According to still further features in the described preferred embodiments the at least one oligonucleotide is attached to a solid substrate.

According to still further features in the described preferred embodiments the solid substrate is configured as a microarray and whereas the at least one oligonucleotide includes a plurality of oligonucleotides each being attached to the microarray in a regio-specific manner.

According to still an additional aspect of the present invention there is provided a method of determining association between a genetic marker and a pathology, the method comprising: (a) identifying a gene having an in-frame stop codon in an intronic sequence thereof; (b) generating a probe capable of specifically hybridizing with a truncated expression product of the gene resultant from the in-frame stop codon; (c) contacting normal and pathological biological samples with the probe; and (d) detecting a level of probe binding in the normal and the pathological biological samples, to thereby determine association between a gene and a pathology.

According to still further features in the described preferred embodiments the truncated expression product is an mRNA and whereas the detecting is effected using an oligonucleotide probe.

According to still further features in the described preferred embodiments the truncated expression product is a polypeptide and whereas the detecting is effected using an antibody probe.

According to a further aspect of the present invention there is provided a method of detecting a presence or absence of an abnormal cellular phenotype associated with a defective transcription machinery, the method comprising: (a) expressing within a cell a recombinant polynucleotide capable of transcribing at least two distinct mRNA transcripts, wherein one of the at least two distinct mRNA transcripts encodes a reporter molecule, whereas a transcript encoding the reporter molecule forms only in cells having the defective transcription machinery; and (b) detecting a presence or absence of the reporter molecule thereby detecting a presence or absence of the abnormal cellular phenotype associated with a defective transcription machinery.

According to still further features in the described preferred embodiments the reporter molecule is selected from the group consisting of a fluorescer, an enzyme and an epitope tag.

According to yet a further aspect of the present invention there is provided a recombinant polynucleotide comprising a nucleic acid sequence being capable of transcribing at least two distinct mRNA transcripts, wherein one of the at least two distinct mRNA transcripts encodes a reporter molecule, whereas a transcript encoding the reporter molecule forms only in cells having a defective transcription machinery.

According to still a further aspect of the present invention there is provided a method of killing cells having abnormal cellular phenotype associated with a defective transcription machinery, the method comprising expressing within the cells a recombinant polynucleotide capable of transcribing at least two distinct mRNA transcripts, wherein one of the at least two distinct mRNA transcripts encodes a peptide toxin, whereas a transcript encoding the peptide toxin forms only in cells having the defective transcription machinery, thereby killing cells having abnormal cellular phenotype associated with the defective transcription machinery.

According to still further features in the described preferred embodiments the peptide toxin is selected from the group consisting of Pseudomonas exotoxin, Diphtheria toxin, Cholera toxin, ricin, abrin, gelonin, pertussis toxin and Shigella toxin.

According to still a further aspect of the present invention there is provided a nucleic acid construct encoding the recombinant polynucleotide of claim 20.

According to still a further aspect of the present invention there is provided a method of treating a genetic disorder associated with a defective transcription machinery in a subject, the method comprising administering to the subject a therapeutically effective amount of a recombinant polynucleotide capable of transcribing at least two distinct mRNA transcripts, wherein one of the at least two distinct mRNA transcripts encodes a peptide toxin, whereas a transcript encoding the peptide toxin forms only in cells having the defective transcription machinery, thereby treating the genetic disorder associated with a defective transcription machinery.

According to still further features in the described preferred embodiments the peptide toxin is selected from the group consisting of Pseudomonas exotoxin, Diphtheria toxin, Cholera toxin, ricin, abrin, gelonin, pertussis toxin and Shigella toxin.

According to still a further aspect of the present invention there is provided a pharmaceutical composition comprising a recombinant polynucleotide capable of transcribing at least two distinct mRNA transcripts, wherein one of the at least two distinct mRNA transcripts encodes a peptide toxin, whereas a transcript encoding the peptide toxin forms only in cells having the defective transcription machinery, and a pharmaceutically acceptable carrier or diluent.

According to still further features in the described preferred embodiments the peptide toxin is selected from the group consisting of Pseudomonas exotoxin, Diphtheria toxin, Cholera toxin, ricin, abrin, gelonin, pertussis toxin and Shigella toxin.

According to still a further aspect of the present invention there is provided a method of treating a genetic disorder associated with abnormal splicing the method comprising fixing mutations associated with premature stop codons thereby treating genetic disorders associated with defective transcription machinery.

According to still further features in the described preferred embodiments the fixing is effected by gene nock-in and whereas the gene nock-in is directed at in-frame stop codons located at intronic sequences.

According to still a further aspect of the present invention there is provided a method of identifying agents which affect the activity of the transcription machinery, the method comprising: (a) expressing in a plurality of cells a recombinant polynucleotide capable of transcribing at least two distinct MRNA transcripts, wherein one of the at least two distinct mRNA transcripts encodes a reporter molecule, whereas a transcript encoding the reporter molecule forms only in cells having the defective transcription machinery; (b) exposing the plurality of cells expressing the recombinant polynucleotide to a plurality of agents; and (c) identifying an agent of the plurality of agents which alters expression of the reporter molecule to thereby identify agents which affect the activity of the transcription machinery.

According to still further features in the described preferred embodiments the agent up-regulates expression of the reporter molecule, to thereby identify agents which damage the transcription machinery.

According to still further features in the described preferred embodiments the agent down-regulates expression of the reporter molecule, to thereby identify agents which repair the transcription machinery.

The present invention successfully addresses the shortcomings of the presently known configurations by providing methods for accurately identifying gene expression products which result from alternative splicing and methods of identifying and treating disorders associated with such genes.

Unless otherwise defined, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs. Although methods and materials similar or equivalent to those described herein can be used in the practice or testing of the present invention, suitable methods and materials are described below. In case of conflict, the patent specification, including definitions, will control. In addition, the materials, methods, and examples are illustrative only and not intended to be limiting.

BRIEF DESCRIPTION OF THE DRAWINGS

The invention is herein described, by way of example only, with reference to the accompanying drawings. With specific reference now to the drawings in detail, it is stressed that the particulars shown are by way of example and for purposes of illustrative discussion of the preferred embodiments of the present invention only, and are presented in the cause of providing what is believed to be the most useful and readily understood description of the principles and conceptual aspects of the invention. In this regard, no attempt is made to show structural details of the invention in more detail than is necessary for a fundamental understanding of the invention, the description taken with the drawings making apparent to those skilled in the art how the several forms of the invention may be embodied in practice.

In the drawings:

FIG. 1 is a schematic illustration of one configuration of the recombinant polynucleotide reporter of the present invention.

FIG. 2 a is a schematic illustration depicting the structure of wild type CAD1 and CAD2 mini genes. Open boxes—exons; Heavy line—intron; narrow box -an intronic sequence included as a part of the exon in the latent RNA. The normal and latent 5′SSs and the in-frame stop codons therebetween are indicated. The S character designates the T nucleotide in a stop codon and the respective distance thereof from the normal 5′SS.

FIGS. 2 b-c are photomicrographs of RT-PCR analyses depicting activation of latent splicing in CAD mutant mini genes devoid of upstream stop codons. Sequences including stop codons and mutations thereof (underlined nucleotides) are indicated above each of the respective lanes; − and + symbols indicate the expected occurrence of latent splicing. Bands corresponding to precursor and mature (i.e., normal and latent) CAD fragments amplified with primers a+b (FIG. 2 b) and primers c+b (FIG. 2 c) are indicated by schematic drawings on the right. These assignments were confirmed by sequence analyses of the DNA fragments extracted from the gel. Note an additional minor band, which is assigned to a heteroduplex between precursor and mature PCR amplified DNAs, occasionally appearing just below the 428 nt band in FIGS. 2 b, 4 b, and 5 b, as confirmed by sequence analyses of the DNA extracted from the gel, and by re-running it on a second gel. Lane 2, control untransfected cells. Lane 1, molecular size markers pBR322 cut with MspI.

FIGS. 3 a-b are photomicrographs of RT-PCR analyses depicting suppression of latent splicing by all in-frame stop codon variants of the CAD pre-mRNA. RT-PCR analyses of CAD constructs were performed with primers a and b (FIG. 3 a) and with primers c and b (FIG. 3 b). Lettering and symbols are as in FIGS. 2 b-c.

FIGS. 4 a-b are photomicrographs of RT-PCR analyses depicting the activation of latent splicing in the CAD mini gene which includes mutations eliminating in-frame stop codons. S86 in CAD2 was frame shifted by an AT insertion at a distance of 53 nt downstream of the normal 5′SS (Mut 6 and Mut 7). All four stop codons in CAD1 (see FIG. 2 b, lane 3) were mutated by a T insertion into S25, thus frame shifting the remaining three (Mut 9). C denotes Control, RNA from untransfected cells. RT-PCR analyses were performed with primers a and b (FIG. 4 a) and with primers c and b (FIG. 4 b). Lettering and symbols are as in FIGS. 2 b-c.

FIGS. 5 a-b are photomicrographs of RT-PCR analyses showing that abrogation of NMD does not Reveal Latent Splicing. FIG. 5 a—Human 293T cells (lanes 1-13) were transfected with CAD mini gene constructs as indicated (lanes 1-4 are co-transfections with pEGFP-N3). 24 hours post-transfection the cultures were treated with cyclohexamide (CHX, 20 μg/ml) for the indicated time periods. RNA was analyzed by RT-PCR as in FIG. 2 b (lettering and symbols are as in FIGS. 2 b-c). FIG. 5 b—Human 293T cells were co-transfected as indicated (β-globin WT, wild type β-globin; β-globin Ter39, a mutant construct expressing β-globin mRNA having a PTC at position 39; CAD Ter, a mutant construct expressing CAD mRNA having a PTC in exon N+1). Treatment with CHX was as in FIG. 5 a. β-globin mRNA was revealed by RT-PCR. Mature CAD 1 and CAD Ter mRNAs were revealed as in FIG. 2 b.

FIG. 6 a is a schematic drawing of wild type IDUA mini genes (symbols are as in FIG. 2 a; S denotes an intronic in-frame stop codon).

FIGS. 6 b-c are photomicrographs of RT-PCR analyses showing that intronic latent 5′ splice site is activated in IDUA mutant mini genes devoid of upstream in-frame stop codons. Gel electrophoretic analyses of RT-PCR DNA fragments obtained from IDUA mini genes. The sequences of the normal 5′SSs in the wild type and the mutant mini genes (mutations underlined) are indicated above each of the respective lanes. Bands corresponding to precursor and mature (normal and latent) IDUA fragments amplified with primers b+c (FIG. 6 b) and primers d+c (FIG. 6 c) are indicated by schematic drawings on the right (other symbols are as in FIGS. 2 b-c). These assignments were confirmed by sequence analyses of the DNA fragments extracted from the gel. The additional minor band that appears just below the 539-nt band in lanes 4-6 of FIG. 6 c was assigned to a heteroduplex between precursor and mature PCR amplified DNAs, as confirmed by sequence analyses of the DNA extracted from the gel, and by re-running it on a second gel. Lane 2, control with RNA from untransfected cells. Lane 1, molecular size markers, pBR322 cut with MspI.

FIGS. 7 a-c illustrate the results of nuclease S1 mapping analysis which show that intronic latent 5′ splice site is activated in CAD mutant mini genes devoid of upstream stop codons. FIG. 7 a—is a map of the 972-bp BsrFI fragment probe and the expected 3′ end labeled fragments protected by the normally spliced CAD RNA (169 nt) and by the latent RNA (294 nt). FIG. 7 b—DNA fragments protected by CAD RNA expressed from CAD2 (lane 2), Mut 1 (lane 3), and Mut 2 (lane 4) constructs. A control of untransfected cells (lane 1) shows no protected DNA fragments of the above size. FIG. 7 c—Nuclease S1 protection experiments were carried out with increasing amounts of input RNA expressed from Mut 1 (lanes 2-4) and from Mut 2 (lanes 5-7). Lane 1 is a control with no input RNA.

FIGS. 8 a-b are schematic illustrations depicting the activation of latent splicing by abrogation of in-frame stop codons. Boxes—exon 1, exon 2; Narrow box—extension of exon 1 resulting from splicing at the latent 5′ splice site; Solid line, intros. Expected splicing patterns are denoted by heavy dotted lines). Splicing at the latent 5′ splice site of the in-frame stop codon-containing pre-mRNA (FIG. 8 a—TGA) is suppressed. Nonsense to sense mutation of this stop codon by either point or frame shift mutation (FIG. 8 b—TGA to TGG or T GA) results in activation of splicing from the downstream latent 5′ splice site.

FIGS. 9 a-c are schematic illustrations depicting splice site sequence patterns. The sequence pattern at the normal 5′ splice sites for introns with internal 5′ splice site consensus sequences (FIG. 9 a) and for introns without internal 5′ splice site consensus sequences (FIG. 9 b), as well as the sequence pattern at the internal intronic 5′ splice site consensus sequences (FIG. 9 c), are represented as weight matrices. The sequence patterns were displayed by using the PICTOGRAM program [http://genes.mit.edu/pictogram.html; Lim and Burge (2001) Proc. Natl. Acad. Sci. USA 98:11193-11198]. The height of each letter is proportional to the frequency of the corresponding base at the given position, and bases are listed in descending order of frequency from top to bottom. The information content (IC in bits) relative to the background of the intron base composition is also shown.

FIG. 10 is a schematic illustration showing wild type HTH, IDUA and CAD mini gene constructs. Open boxes—exons; Lines—introns; Narrow boxes—intronic sequence included as part of the exon in latent RNA; Diagonal lines—normal splicing patterns. The normal and latent 5′ splice sites and the in-frame stop codons between them are indicated (S# designates the T nucleotide in a stop codon and its respective distance from the normal 5′ splice site).

FIG. 11 a is a schematic illustration of the wild type HTH mini-gene (schematics as in FIG. 10) and a blowup of exons 1 and 1a, showing the sequence and reading frame of exon 1a, and the alternative splicing patterns (diagonal lines).

FIGS. 11 b-c are photomicrographs showing that an alternative 5′SS in the first exon of the HTH gene is suppressed by the introduction of an upstream in-frame stop codon. FIG. 11 b—is an RT-PCR analysis of HTH transcripts, expressed from wild type and mutant constructs. The sequence of codon 4 in the wild type and the mutant mini genes, and the expected occurrence of splicing at 5′ splice site 1a (±), are indicated above each lane. Bands of RT-PCR fragments corresponding to the alternatively spliced HTH RNAs are indicated by schematic drawings, on the left. RT-PCR fragments were amplified with primers n+f, and revealed by Southern blotting using ³²P-labeled antisense HTH RNA as a probe. FIG. 11 c—are RT-PCR fragments of FIG. 11 b as visualized by ethidium bromide staining.

FIGS. 12 a-b are photomicrographs showing that the presence of the translation inhibitor CHX does not effect latent splicing of HTH wild type or Mut 1 (FIG. 12 a) and IDUA wild type or Mut 1 constructs (FIG. 12 b) as indicated. Twenty-four hours post-transfection the cell cultures were treated with cycloheximide (CHX, 20 mg/ml, for the indicated lengths of time). RT-PCR was performed with primers n+f (FIG. 12 a) or b+c (FIG. 12 b).

FIGS. 13 a-b are photomicrographs showing that the presence of G418 does not effect latent splicing of HTH wild type or Mut 1 (FIG. 13 a) and IDUA wild type or Mut 1 constructs (FIG. 13 b) as indicated. Cells were treated for 18 hours with the Indicated concentrations of G418. RT-PCR was performed with primers n+f (FIG. 13 a) or b+c (FIG. 13 b).

FIGS. 14 a-d are photomicrographs showing that suppressor tRNA is unable to activate latent splicing. Mini gene constructs of wild type and mutant of CAD (FIG. 14 a), HTH (FIG. 14 b) and IDUA (FIG. 14 c) were each co-transfected with GFP and the respective cognate suppressor tRNA, and RT-PCR was performed. Control experiments using a wild type and β-globin Ter39 constructs showed that the cognate suppressor tRNA was able to abrogate NMD under the same conditions (FIG. 14 d).

FIGS. 15 a-d are photomicrographs showing that dominant negative mutant of hUpf1 is unable to activate latent splicing. Mini gene constructs of wild type and mutant of CAD (FIG. 15 a), HTH (FIG. 15 b) and IDUA (FIG. 15 c) were each co- transfected with GFP and with either hUpf1 wild type or its dominant negative mutant construct as indicated, and analyzed by RT-PCR. The band at ˜500 in FIG. 15 c, lanes 1-3, is a heteroduplex, as confirmed by denaturing gel analysis. Control experiments with β-globin constructs showed that the dominant negative mutant of hUpf1 was able to abrogate NMD under the same conditions (FIG. 15 d).

DESCRIPTION OF THE PREFERRED EMBODIMENTS

The present invention is of methods of identifying gene expression products, which can be used to identify pathogenic genes such as oncogenes. Specifically, the present invention can be used to diagnose and treat diseases associated with the expression of such pathogenic genes, such as cancer.

The principles and operation of the present may be better understood with reference to the drawings and accompanying descriptions.

Before explaining at least one embodiment of the invention in detail, it is to be understood that the invention is not limited in its application to the details set forth in the following description or exemplified by the Examples. The invention is capable of other embodiments or of being practiced or carried out in various ways. Also, it is to be understood that the phraseology and terminology employed herein is for the purpose of description and should not be regarded as limiting.

Alternative splicing, the process by which multiple mRNA isoforms are generated from a single pre-mRNA species is an important means of regulating gene expression. The accuracy and efficiency of pre-mRNA splicing is governed by a number of trans-acting factors and cis acting sequence elements.

A key step in pre-mRNA splicing involves the recognition and selection of a consensus sequence AG/GTRAGT (wherein R denotes a purine and “/” denotes the splice junction, SEQ ID NO: 1) at the 5′ splice site [5′SS, Black (1995) RNA 1:763-771; Kramer (1996) Annu. Rev. Biochem. 65:367-409; Burge (1999) in The RNA World, 2^(nd) edition, eds. Gesteland C B., Cech T R., and Atkins J F., (Cold Spring Harbor Press, Cold Spring Harbor, N.Y.)]. Frequently, however, 5′SS which comply with the consensus are not selected for splicing [i.e., ‘latent 5′SS’, Green (1 991) Annu. Rev. Biochem. 65:367-409], suggesting that the splicing machinery distinguishes between normal and latent 5′SSs. To date, parameters used for identifying latent 5′SSs are not known.

While reducing the present invention to practice the present inventors have uncovered that intronic in-frame stop codons located upstream to 5′SS sequence render the such splice site sequences latent.

As described hereinbelow and in the Examples section which follows the present inventors illustrate that elimination of in-frame stop codons located upstream of latent 5′ splice sites activated splicing in the CAD and IDUA genes (GeneBank Accession Nos. M31621.1 and AH002600.1, respectively, see Examples 1-4) and further that introduction of an in-frame stop codon between two adjacent alternative 5′ splice sites which are normally used to express splice variants of the HTH gene (GeneBank Accession No. D00269.1) abolished splicing from the downstream site (see Example. 6), substantiating the effect of intronic in-frame stop codons on latent splicing.

Thus, the findings presented herein provide, for the first time, guidelines which can be used to accurately predict gene expression products in-silico.

Thus, according to one aspect of the present invention there is provided a method of uncovering latent splice sites.

As used herein the phrase “latent splice sites” refers to intron splice sites from which splicing is suppressed under normal cellular conditions.

The method is effected by identifying at least one intronic in-frame stop codon located upstream of a 5′ splice site sequence, wherein such 5′ splice sequence is a latent splice site to thereby uncover latent splice sites.

As used herein an “intronic in-frame stop codon” refers to a stop codon such as UAA, UAG or UGA which is located in an intron sequence but maintains the open reading frame of the preceding upstream exon. The intronic in-frame stop codons of this aspect of the present invention are typically flanked by an upstream normal 5′SS and a downstream latent 5′SS. Methods of identifying an open reading frame are well known in the art.

Identification of intronic in-frame stop codons which are located upstream of 5′SSs can be effected manually or using suitable software applications such as operable on a PC machine. Such software applications are well known in the art. Examples include but are not limited to the Motif software of the GCG package (Genetics Computer Group, Wisconsin), Macvector (available from www.accelrvs.com/products/macvector/), DNASIS (available from Hitachi software engineering, Inc.), GeneMine (available from Molecular Application Group, Inc.), LaserGene (available from DNAStar Inc.) and Omiga (available from Oxford Molecular Group, Inc.).

Using the methodology of this aspect of the present invention, the present inventors uncovered that 95.8% of latent splice sites include at least one in-frame stop codon in the upstream intronic sequence (see Example 5 of the Examples section).

The hereinabove described methodology can be applied in a large scale to identify latent splice sites even at the level of a whole genome or transcriptom. Once genes including such latent splice sites are identified they can be stored in a database which can be generated by a suitable computing platform.

It is conceivable that 5′SS located downstream of intronic in-frame stop codons are rendered latent to avoid inclusion of stop codons in the reading frame of the expression product thereby leading to premature termination of the protein product (i.e., truncated proteins). Thus, the present invention suggests a general surveillance mechanism which role is to identify in-frame stop codons and suppress splicing (SOS) at latent downstream 5′SS such that the deleterious effects of premature termination codons (PTCs) in apparently wild-type transcripts are avoided.

Such a surveillance mechanism has been previously described for the nonsense mediated mRNA decay (NMD) pathway, which ensures the degradation of nonsense mRNAs [Frischmeyer and Dietz (1999) Hum. Mol. Genet. 8:1893-1900; Hentze and Kulozik (1999) Cell 96:307-310; Li and Wilkinson (1998) Immunity 8:135-141 and Maquat (2002) Genes Dev. 16:1743-1753]. However, in sharp contrast, the SOS mechanism of the present invention does not seem to involve ribosomes since it is not affected by either the protein synthesis inhibitor cyclohexamide (CHX) or the aminoglycoside antibiotic G-418, which allows stop codon read-through (see Examples 3-4 of the Examples section). Furthermore, latent splicing is not activated in the presence of a suppressor tRNA which also allow stop codon readthrough nor is it activated in the presence of a dominant negative mutant of the NMD gene, hUpf1 [GenBank Accession No. U59323, Sun (1998) Proc. Natl. Acad. Sci. USA 95:10009-10014, see Example 6 of the Examples section]. These findings suggest that SOS has a different mechanism than NMD.

The nuclear scanning mechanism identified and characterized herein can be harnessed, for example to generate within cells, which are characterized by a defective nuclear scanning mechanism, alternative transcripts from a single coding sequence. Such alternative transcripts can exhibit distinct characteristics to be utilized in diagnostic and therapeutic applications.

Thus, according to another aspect of the present invention there is provided a method of detecting a presence or absence of an abnormal cellular phenotype which is associated with a defective transcription machinery.

As used herein the phrase “defective transcription machinery” refers to cellular mechanisms which ensure transcript quality. Examples include but are not limited to the nuclear scanning mechanism described hereinabove, the splicing machinery such as the SR proteins described hereinabove and the nonsense mediated mRNA decay (NMD) machinery.

The method is effected by expressing within a cell a recombinant polynucleotide capable of transcribing at least two mRNA transcripts, wherein one of the at least two distinct mRNA transcripts encodes a reporter molecule, which forms only in cells having the transcription machinery.

Once the recombinant polynucleotide is expressed, the presence or absence of the reporter molecule in the cell is detected to thereby detect the presence or absence of the abnormal cellular phenotype which is associated with the defective transcription machinery.

As used herein the phrase “recombinant polynucleotide” refers to a polynucleotide sequence which includes at least two otherwise separated nucleic acid sequence segments, generated using molecular biology techniques.

The recombinant polynucleotide of this aspect of the present invention can have numerous configurations. One representative configuration is illustrated in FIG. 1 wherein, the recombinant polynucleotide of this aspect of the present invention includes a first exon followed by an intron which includes an in-frame stop codon flanked by two 5′SSs and a downstream 3′SS and a second exon, which includes an in-frame stop codon. An in-frame intronic reporter molecule is positioned upstream of the in-frame intronic stop codon. Such a recombinant polynucleotide encodes under normal conditions an expression product, which includes exon 1 and exon 2 only. However, under pathological conditions (e.g., viral infection, exposure to mutagens and the like) a fusion protein including exon 1 followed by a down stream reporter molecule would be expressed.

It will be appreciated that the recombinant polynucleotides of this aspect of the present invention can also be used to identify agents, which affect the activity of the transcription machinery. The method of this aspect of the present invention is effected by exposing the cells which express the recombinant polynucleotides of the present invention to a plurality of agent and determining which agent is capable of altering the expression of the reporter molecule to thereby identify agents, which affect the activity of the transcription machinery. The method can identify agents which upregulate expression of the reporter molecule, thereby identifying agents which damage the transcription machinery. Alternatively the method can identify agents which down regulate expression of the reporter molecule in a transcription defective cell, thereby identifying agents which repair the transcription machinery, such agents can be used in numerous therapeutic applications.

Agents, which can be utilized according to the present invention include, can include small molecules, such as, for example, naturally occurring compounds (e.g., compounds derived from plant extracts, microbial broths, and the like) or synthetic organic or organometallic compounds; mutagenic agents can also include viruses and microorganisms such as bacteria and intracellular parasites.

Various growth conditions can also be used as agents of this aspect of the present invention. Conditions suitable for use as putative mutagens according to the present invention include, but are not limited to, temperature, humidity, atmospheric pressure, gas concentrations, growth media, contact surfaces, radiation exposure (such as, gamma radiation, UV radiation, X-radiation) and the presence or absence of other cells in a culture.

The reporter molecule of the present invention can be a polypeptide label which can be quantitated directly or indirectly. For example, a polypeptide label can be an enzyme which when in the presence of a suitable substrate generates chromogenic products. Such enzymes include but are not limited to alkaline phosphatase, β-galactosidase, β-D-glucoronidase (GUS) and the like. A polypeptide label can also be a fluorescer such as the polypeptides belonging to the green fluorescent protein family including the green fluorescent protein, the yellow fluorescent protein, the cyan fluorescent protein and the red fluorescent protein as well as their enhanced derivatives. In such case, the polypeptide label can be quantified via its fluorescence, which is generated upon the application of a suitable excitatory light. Alternatively, a polypeptide label can be an epitope tag, a fairly unique polypeptide sequence to which a specific antibody can bind without substantially cross reacting with other cellular epitopes. Such epitope tags include a Myc tag, a Flag tag, a His tag, a Leucine tag, an IgG tag, a streptavidin tag and the like. Further detail of polypeptide labels can be found in Misawa et al. (2000) Proc. Natl. Acad. Sci. USA 97:3062-3066

Alternatively the reporter molecule can be a nucleic acid molecule such as a reporter mRNA molecule. For example an amplifiable nucleic acid sequence can be used as a reporter molecule, provided that it is a unique sequence included only in the reporter segment of the recombinant polynucleotide (see for example U.S. Pat. No. 6,369,207).

As mentioned hereinabove the recombinant polynucleotide is expressed within a cell. The cell according to this aspect of the present invention is preferably a eukartyotic cell which includes a functional or dysfunctional transcription (e.g., splicing) machinery and which is readily propagatable in culture. Cells of this aspect of the present invention can be recovered from an abnormal tissue such as a tumor tissue or can be chemically or genetically (e.g., site directed mutagenesis) induced using laboratory techniques known in the art.

Typically, the recombinant polynucleotide of the present invention is expressed from a nucleic acid expression construct. Such an expression construct further includes at least one cis acting regulatory element. As used herein, the phrase “cis acting regulatory element” refers to a polynucleotide sequence, preferably a promoter, which binds a trans acting regulator and regulates the transcription of a coding sequence located downstream thereto.

Any available promoter can be used by the present methodology. In a preferred embodiment of the present invention, the promoter utilized by the nucleic acid construct of the present invention is active in the specific cell population transformed. Examples of cell type-specific and/or tissue-specific promoters include promoters such as albumin that is liver specific [Pinkert et al., (1987) Genes Dev. 1:268-277], lymphoid specific promoters [Calame et al., (1988) Adv. Immunol. 43:235-275]; in particular promoters of T-cell receptors [Winoto et al., (1989) EMBO J. 8:729-733] and immunoglobulins; [Banerji et al. (1983) Cell 33729-740], neuron-specific promoters such as the neurofilament promoter [Byrne et al. (1989) Proc. Natl. Acad. Sci. USA 86:5473-5477], pancreas-specific promoters [Edlunch et al. (1985) Science 230:912-916] or mammary gland-specific promoters such as the milk whey promoter (U.S. Pat. No. 4,873,316 and European Application Publication No. 264,166). The nucleic acid construct of the present invention can further include an enhancer, which can be adjacent or distant to the promoter sequence and can function in up regulating the transcription therefrom.

The constructs of the present methodology preferably further include an appropriate selectable marker and/or an origin of replication. Preferably, the construct utilized is a shuttle vector, which can propagate both in E. coli (wherein the construct comprises an appropriate selectable marker and origin of replication) and be compatible for propagation in cells, or integration in a gene and a tissue of choice.

The construct according to the present invention can be, for example, a plasmid, a bacmid, a phagemid, a cosmid, a phage, a virus or an artificial chromosome.

Methods of introducing the recombinant polynucleotides of the present invention into eukaryotic cells are well known in the art. Examples include but are not limited to transfection, infection, conjugation, electroporation, calcium phosphate-precipitation, direct microinjection, liposome fusion and the like. Selection of a suitable introduction method is dependent upon the host cell and the nucleic acid construct used.

Since abnormal transcripts which exhibit nonsense mutations such as premature stop codons are normally identified by the nonsense-mediated mRNA decay (NMD) machinery which functions to degrade non-functional or deleterious transcripts, measures are taken to prevent the activation of such RNA degradation machinery, thereby allowing optimal accumulation of the expression products within the cell. Examples of NMD inhibitors include but are not limited to cyclohexamide.

Following expression, cells, which exhibit reporter activity are identified preferably by comparing these cells to similar cells, which were not introduced with the recombinant polynucleotide of the present invention. Methods of identifying such reporter activity are well known in the art. For example, in cases where a fluorescent reporter is used reporter activity is identified using a variety of microscopic visualization techniques which are well known in the art.

It will be appreciated that, once a cell with a defective transcription machinery is identified it can be used to uncover novel genes which constitute the transcription machinery such as genes which comprise the nuclear scanning mechanism. Identification of such genes can be effected using molecular biology techniques which are well known in the art. Examples include but are not limited to differential display technique [Liang and Pardee (1992) Science 257:967-70; Welsh et al. (1992) Nucleic Acids Res. 20:4965-70], subtractive cloning [Buckbinder (1994) Proc. Natl. Acad. Sci. USA 91:10640-10644] and serial analysis of gene expression (SAGE) [Valculescu et al. (1995) Science 270:484-8].

It is well known that defective transcription machinery, which results predominantly in immediate truncation, splicing abnormalities or altered reading frames producing grossly truncated proteins is directly correlated with the development of genetic diseases and cancer. For example, a nonsense mutation in exon 51 of the fibrillin 1 (FBN1) gene is associated with exon skipping and causes Marfan syndrome [Dietz (1993) Science 259:680-683], other examples include Duchenne muscular dystrophy, and Becker muscular dystrophy which are caused by mutations in the dystrophyn gene [DMD, Ahn (1993) Nature Genet. 3:283-291].

Thus, once cells which are characterized by defective transcription machinery, are identified they are preferably eliminated.

Thus, according to yet another aspect of the present invention there is provided a method of killing cells having abnormal cellular phenotype associated with a defective transcription machinery.

The method is effected by expressing within the cells a recombinant polynucleotide which is capable of transcribing at least two distinct mRNA transcripts, such as described hereinabove, however rather than a reporter molecule, a peptide toxin is formed only in cells with the defective transcription machinery to thereby kill such cells.

Examples of peptide toxins which can be used by the present methodology include but are not limited to cholera toxin, botulinum toxin, anthrax toxin, diphteria toxin, pertussis toxin, shigella toxin pseudomonas exo-toxin and the like (see U.S. Pat. Nos. 6,399,078, 6,221,397, 6,051,238 and 5,980,898).

The recombinant polynucleotides of the present invention can be used to diagnose and treat genetic disorders which are associated with a defective transcription machinery in a subject. Preferred individual subjects according to the present invention are mammals such as canines, felines, ovines, porcines, equines, bovines and humans.

The recombinant polynucleotides of the present invention can be provided to an individual per se, or as part of a pharmaceutical composition where it is mixed with a pharmaceutically acceptable carrier.

As used herein a “pharmaceutical composition” refers to a preparation of one or more of the active ingredients described herein with other chemical components such as physiologically suitable carriers and excipients. The purpose of a pharmaceutical composition is to facilitate administration of a compound to an organism.

Herein the term “active ingredient” refers to the recombinant polynucleotide preparation, which is accountable for the biological effect.

Hereinafter, the phrases “physiologically acceptable carrier” and “pharmaceutically acceptable carrier” which may be interchangeably used refer to a carrier or a diluent that does not cause significant irritation to an organism and does not abrogate the biological activity and properties of the administered compound. An adjuvant is included under these phrases. One of the ingredients included in the pharmaceutically acceptable carrier can be for example polyethylene glycol (PEG), a biocompatible polymer with a wide range of solubility in both organic and aqueous media (Mutter et al. (1979).

Herein the term “excipient” refers to an inert substance added to a pharmaceutical composition to further facilitate administration of an active ingredient. Examples, without limitation, of excipients include calcium carbonate, calcium phosphate, various sugars and types of starch, cellulose derivatives, gelatin, vegetable oils and polyethylene glycols.

Techniques for formulation and administration of drugs may be found in “Remington's Pharmaceutical Sciences,” Mack Publishing Co., Easton, Pa., latest edition, which is incorporated herein by reference.

Suitable routes of administration may, for example, include oral, rectal, transmucosal, especially transnasal, intestinal or parenteral delivery, including intramuscular, subcutaneous and intramedullary injections as well as intrathecal, direct intraventricular, intravenous, inrtaperitoneal, intranasal, or intraocular injections.

Alternately, one may administer a preparation in a local rather than systemic manner, for example, via injection of the preparation directly into a specific region of a patient's body.

Pharmaceutical compositions of the present invention may be manufactured by processes well known in the art, e.g., by means of conventional mixing, dissolving, granulating, dragee-making, levigating, emulsifying, encapsulating, entrapping or lyophilizing processes.

Pharmaceutical compositions for use in accordance with the present invention may be formulated in conventional manner using one or more physiologically acceptable carriers comprising excipients and auxiliaries, which facilitate processing of the active ingredients into preparations which, can be used pharmaceutically. Proper formulation is dependent upon the route of administration chosen.

For injection, the active ingredients of the invention may be formulated in aqueous solutions, preferably in physiologically compatible buffers such as Hank's solution, Ringer's solution, or physiological salt buffer. For transmucosal administration, penetrants appropriate to the barrier to be permeated are used in the formulation. Such penetrants are generally known in the art.

For oral administration, the compounds can be formulated readily by combining the active compounds with pharmaceutically acceptable carriers well known in the art. Such carriers enable the compounds of the invention to be formulated as tablets, pills, dragees, capsules, liquids, gels, syrups, slurries, suspensions, and the like, for oral ingestion by a patient. Pharmacological preparations for oral use can be made using a solid excipient, optionally grinding the resulting mixture, and processing the mixture of granules, after adding suitable auxiliaries if desired, to obtain tablets or dragee cores. Suitable excipients are, in particular, fillers such as sugars, including lactose, sucrose, mannitol, or sorbitol; cellulose preparations such as, for example, maize starch, wheat starch, rice starch, potato starch, gelatin, gum tragacanth, methyl cellulose, hydroxypropylmethyl-cellulose, sodium carbomethylcellulose; and/or physiologically acceptable polymers such as polyvinylpyrrolidone (PVP). If desired, disintegrating agents may be added, such as cross-linked polyvinyl pyrrolidone, agar, or alginic acid or a salt thereof such as sodium alginate.

Dragee cores are provided with suitable coatings. For this purpose, concentrated sugar solutions may be used which may optionally contain gum arabic, talc, polyvinyl pyrrolidone, carbopol gel, polyethylene glycol, titanium dioxide, lacquer solutions and suitable organic solvents or solvent mixtures. Dyestuffs or pigments may be added to the tablets or dragee coatings for identification or to characterize different combinations of active compound doses.

Pharmaceutical compositions, which can be used orally, include push-fit capsules made of gelatin as well as soft, sealed capsules made of gelatin and a plasticizer, such as glycerol or sorbitol. The push-fit capsules may contain the active ingredients in admixture with filler such as lactose, binders such as starches, lubricants such as talc or magnesium stearate and, optionally, stabilizers. In soft capsules, the active ingredients may be dissolved or suspended in suitable liquids, such as fatty oils, liquid paraffin, or liquid polyethylene glycols. In addition, stabilizers may be added. All formulations for oral administration should be in dosages suitable for the chosen route of administration.

For buccal administration, the compositions may take the form of tablets or lozenges formulated in conventional manner.

For administration by nasal inhalation, the active ingredients for use according to the present invention are conveniently delivered in the form of an aerosol spray presentation from a pressurized pack or a nebulizer with the use of a suitable propellant, e.g., dichlorodifluoromethane, trichlorofluoromethane, dichloro-tetrafluoroethane or carbon dioxide. In the case of a pressurized aerosol, the dosage unit may be determined by providing a valve to deliver a metered amount. Capsules and cartridges of, e.g., gelatin for use in a dispenser may be formulated containing a powder mix of the compound and a suitable powder base such as lactose or starch.

The preparations described herein may be formulated for parenteral administration, e.g., by bolus injection or continuous infusion. Formulations for injection may be presented in unit dosage form, e.g., in ampoules or in multidose containers with optionally, an added preservative. The compositions may be suspensions, solutions or emulsions in oily or aqueous vehicles, and may contain formulatory agents such as suspending, stabilizing and/or dispersing agents.

Pharmaceutical compositions for parenteral administration include aqueous solutions of the active preparation in water-soluble form. Additionally, suspensions of the active ingredients may be prepared as appropriate oily or water based injection suspensions. Suitable lipophilic solvents or vehicles include fatty oils such as sesame oil, or synthetic fatty acids esters such as ethyl oleate, triglycerides or liposomes. Aqueous injection suspensions may contain substances, which increase the viscosity of the suspension, such as sodium carboxymethyl cellulose, sorbitol or dextran. Optionally, the suspension may also contain suitable stabilizers or agents which increase the solubility of the active ingredients to allow for the preparation of highly concentrated solutions.

Alternatively, the active ingredient may be in powder form for constitution with a suitable vehicle, e.g., sterile, pyrogen-free water based solution, before use.

The preparation of the present invention may also be formulated in rectal compositions such as suppositories or retention enemas, using, e.g., conventional suppository bases such as cocoa butter or other glycerides.

Pharmaceutical compositions suitable for use in context of the present invention include compositions wherein the active ingredients are contained in an amount effective to achieve the intended purpose. More specifically, a therapeutically effective amount means an amount of active ingredients effective to prevent, alleviate or ameliorate symptoms of disease or prolong the survival of the subject being treated.

Determination of a therapeutically effective amount is well within the capability of those skilled in the art.

For any preparation used in the methods of the invention, the therapeutically effective amount or dose can be estimated initially from in vitro assays. For example, a dose can be formulated in animal models and such information can be used to more accurately determine useful doses in humans.

Toxicity and therapeutic efficacy of the active ingredients described herein can be determined by standard pharmaceutical procedures in vitro, in cell cultures or experimental animals. The data obtained from these in vitro and cell culture assays and animal studies can be used in formulating a range of dosage for use in human. The dosage may vary depending upon the dosage form employed and the route of administration utilized. The exact formulation, route of administration and dosage can be chosen by the individual physician in view of the patient's condition. [See e.g., Fingl, et al., (1975) “The Pharmacological Basis of Therapeutics”, Ch. 1 p.1].

Depending on the severity and responsiveness of the condition to be treated, dosing can be of a single or a plurality of administrations, with course of treatment lasting from several days to several weeks or until cure is effected or diminution of the disease state is achieved.

The amount of a composition to be administered will, of course, be dependent on the subject being treated, the severity of the affliction, the manner of administration, the judgment of the prescribing physician, etc.

Compositions including the preparation of the present invention formulated in a compatible pharmaceutical carrier may also be prepared, placed in an appropriate container, and labeled for treatment of an indicated condition.

Compositions of the present invention may, if desired, be presented in a pack or dispenser device, such as an FDA approved kit, which may contain one or more unit dosage forms containing the active ingredient. The pack may, for example, comprise metal or plastic foil, such as a blister pack. The pack or dispenser device may be accompanied by instructions for administration. The pack or dispenser may also be accommodated by a notice associated with the container in a form prescribed by a governmental agency regulating the manufacture, use or sale of pharmaceuticals, which notice is reflective of approval by the agency of the form of the compositions or human or veterinary administration. Such notice, for example, may be of labeling approved by the U.S. Food and Drug Administration for prescription drugs or of an approved product insert.

Currently preferred in vivo nucleic acid transfer techniques include transfection with viral or non-viral constructs, such as adenovirus, lentivirus, Herpes simplex I virus, or adeno-associated virus (AAV) and lipid-based systems. Useful lipids for lipid-mediated transfer of the gene are, for example, DOTMA, DOPE, and DC-Chol [Tonkinson et al., Cancer Investigation, 14(1): 54-65 (1996)].

Preferred constructs for use in-vivo applications are viruses, most preferably adenoviruses, AAV, lentiviruses, or retroviruses. A viral construct such as a retroviral construct includes at least one transcriptional promoter/enhancer or locus-defining element(s), or other elements that control gene expression by other means such as alternate splicing, nuclear RNA export, or post-translational modification of messenger. Such vector constructs also include a packaging signal, long terminal repeats (LTRs) or portions thereof, and positive and negative strand primer binding sites appropriate to the virus used, unless it is already present in the viral construct. By way of example, such constructs will typically include a 5′ LTR, a tRNA binding site, a packaging signal, an origin of second-strand DNA synthesis, and a 3′ LTR or a portion thereof. Other vectors can be used that are non-viral, such as cationic lipids, polylysine, and dendrimers.

Preferred modes for in-vivo nucleic acid delivery protocols are provided in Somia and Verma (2000) Nature Reviews 1:91-99, Isner (2002) Myocardial gene therapy Nature 415:234-239; High (2001) Gene therapy: a 2001 perspective. Haemophilia 7:23-27; and Hammond and McKirnan (2001) Angiogenic gene therapy for heart disease: a review of animal studies and clinical trials. 49:561-567.

Genetic disorders are frequently caused by mutations in normal cellular genes which control development, growth and differentiation. For example, the tumorigenic process involves an interplay between at least two classes of genes: oncogenes and tumor suppressor genes. Abnormal activation of oncogenes which promote cell proliferation and/or inactivation of tumor suppressor genes result in tumor formation or progression.

Despite remarkable advances in DNA technology and the completion of the first draft of the human genome, only very limited number of genes which control disease development and progression is currently known.

As is describes hereinabove the present inventors have uncovered a new class of genes which are characterized by an in-frame intronic stop codon. Expression of such genes can lead under special circumstances to the generation of truncated and potentially harmful protein products and thus can be considered as putative pathogenic genes.

Thus according to still another aspect of the present invention, there is provided a method of identifying putative pathogenic genes.

As used herein the phrase “pathogenic genes” refers to genes which abnormal expression thereof results in a genetic disease, such as proto-oncogenes and tumor suppressor genes.

The method according to this aspect o the present invention is effected by identifying an in-frame stop codon in an intronic sequence of a gene, thereby identifying the putative pathogenic genes.

The in-frame stop codons in intronic sequences of this aspect of the present invention may lead to truncated expression products, such as occurring in the absence of a functional nuclear scanning mechanism or a functional nonsense mediated mRNA decay machinery.

Identification of in-frame stop codons in intronic sequences is preferably effected on gene sequences which include introns, such as genomic DNA sequences, contigs or pre-mRNA sequences. Such sequences can be retrieved from nucleic acid sequence databases which are prepared from specific tissues or cell-lines or from whole organisms.

Identification of intron sequences may be effected based on pre-determined annotations, however since sequence annotations from publicly available databases is oftentimes unreliable, further validation of intron-exon boundaries is preferably effected based on intron exon conserved sequences, such as 5′SS, 3′SS, polypyrimidine tract and the like [Roscigno, R., F. et al., (1993) J. Biol. Chem. 268:11222-11229 and the Background section].

Once putative pathogenic gene sequences are identified they are preferably stored in a database which can be generated by a suitable computing platform.

Optionally, expression of truncated expression products resultant from such putative pathogenic genes is detected in a pathogenic tissue to uncover genes which are associated with a pathogenic tissue.

Identification of such truncated expression products may be effected using computer based techniques. For example, in-frame intronic stop codon can be identified in a database of expressed polynucleotide sequences, using computer dedicated software described hereinabove.

Such a database can be a pre-existing publicly available database [i.e., GenBank database maintained by the National Center for Biotechnology Information (NCBI), part of the National Library of Medicine, and the TIGR database maintained by The Institute for Genomic Research] or private databases (i.e., the LifeSeq.™ and PathoSeq.™ databases available from Incyte Pharmaceuticals, Inc. of Palo Alto, Calif.).

Alternatively, the database can be generated from sequence libraries including, but not limited to, cDNA libraries, EST libraries, mRNA libraries and the like.

Construction and sequencing of a cDNA library is one approach for generating a database of expressed mRNA sequences. cDNA library construction is typically effected by tissue or cell sample preparation, RNA isolation, cDNA sequence construction and sequencing.

It will be appreciated that such cDNA libraries can be constructed from RNA isolated from whole organisms, tissues, tissue sections, or cell populations. Libraries are preferably constructed from a tissue reflecting a particular pathological or physiological state which is, for example, associated with genetic aberrations.

For example, libraries can be constructed from hematological malignancies including leukemia and lymphoma. Examples of such libraries include the human chronic myelogenous leukemia Creator™ Smart™ cDNA library and human acute myelogenous leukemia Creator™ Smart™ cDNA library (Cat. Nos. HL9507DD and HL9506DD, respectively Clontech Inc.).

Alternatively, identification of truncated expression products can be effected using well known molecular biology (e.g., hybridization assay such as northern blot, dot blot, RNase protection assay, RT-PCR and the like) and/or biochemical (i.e., protein gel electrophoresis, western blot and the like) techniques.

For example, antibodies or antibody fragments can be used to detect truncated expression products. For example, when an antibody is directed at a truncated polypeptide region a presence or absence of signal will be indicative of an intact protein (i.e., presence signal) or a truncated product thereof (i.e., absence signal).

Alternatively, antibodies directed at a region which is shared by the intact and truncated polypeptide product can be used to detect the truncation however additional parameters such as migration of the immunocomplex on an SDS-PAGE should be applied.

The use of immunological reagents for detecting particular proteins in samples using such reagents are described in current protocols in immunology, Coligan et al., Eds., John Wiley & Sons, New York (1995); Volume 2, Chapter 14 of current protocols in molecular biology, Ausubel et al., Eds., John Wiley & Sons, Inc. (1994); and Linnoila et al., A.J.C.P. 97(2): 235-243 (1992) and Peri et al., J. Clin. Invest. 92: 2099-2109 (1992).

Methods of generating antibodies (i.e., monoclonal and polyclonal) are well known in the art. Antibodies may be generated via any one of several methods known in the art, which methods can employ induction of in vivo production of antibody molecules, screening immunoglobulin libraries or panels of highly specific binding reagents as disclosed [Orlandi D. R. et al. (1989) Proc. Natl. Acad. Sci. 86:3833-3837, Winter G. et al. (1991) Nature 349:293-299] or generation of monoclonal antibody molecules by continuous cell lines in culture. These include but are not limited to, the hybridoma technique, the human B-cell hybridoma technique, and the Epstein-Bar-Virus (EBV)-hybridoma technique [Kohler G., et al. (1975) Nature 256:495-497, Kozbor D., et al. (1985) J. Immunol. Methods 81:31-42, Cote R. J. et al. (1983) Proc. Natl. Acad. Sci. 80:2026-2030, Cole S. P. et al. (1984) Mol. Cell. Biol. 62:109-120]; Antibody fragments can be obtained using methods well known in the art. (See for example, Harlow and Lane, Antibodies: A Laboratory Manual, Cold Spring Harbor Laboratory, New York, 1988, incorporated herein by reference).

Alternatively, an mRNA expression product including an in-frame intronic stop codon can be identified using an oligonucleotide which includes a nucleic acid sequence specifically hybridizable with the in-frame intronic stop codon.

To specifically hybridize with the in-frame intronic stop codon the oligonucleotide probe of the present invention is preferably designed to hybridize with the stop codon and sequences flanking thereof. For example, an oligonucleotide probe capable of specifically hybridizing with a truncated CAD expression product is set forth in SEQ ID NO: 31.

The oligonucleotides of the present invention can be of varying lengths such as between 10-100 base pairs and are preferably purine rich to increase hybridization stringency (i.e., purine content is higher than 50%).

In general, the oligonucleotides of the present invention may be generated by any oligonucleotide synthesis method known in the art such as enzymatic synthesis or solid phase synthesis. Equipment and reagents for executing solid-phase synthesis are commercially available from, for example, Applied Biosystems. Any other means for such synthesis may also be employed; the actual synthesis of the oligonucleotides is well within the capabilities of one skilled in the art and as such is not further described herein.

Probes generated according to the teachings of the present invention can be used to determine an association between a genetic marker and a pathology.

First, a gene having an in-frame stop codon in an intronic sequence thereof is identified. Then, probes capable of specifically hybridizing with a truncated expression product of the gene resultant of the in-frame stop codon are generated, such as described hereinabove. Such probes are contacted with normal and pathological biological samples and a level of probe binding to these samples is determined to thereby determine association between a gene and a pathology.

For example, contacting of the oligonucleotide probes of the present invention with the biological sample is effected by stringent, moderate or mild hybridization (as used in any polynucleotide hybridization assay such as northern blot, dot blot, RNase protection assay, RT-PCR and the like). Wherein stringent hybridization is effected by a hybridization solution of 6×SSC and 1% SDS or 3 M TMACI, 0.01 M sodium phosphate (pH 6.8), 1 mM EDTA (pH 7.6), 0.5% SDS, 100 μg/ml denatured salmon sperm DNA and 0.1% nonfat dried milk, hybridization temperature of 1-1.5 ° C. below the T_(m), final wash solution of 3 M TMACI, 0.01 M sodium phosphate (pH 6.8), 1 mM EDTA (pH 7.6), 0.5% SDS at 1-1.5° C. below the T_(m); moderate hybridization is effected by a hybridization solution of 6×SSC and 0.1% SDS or 3 M TMACI, 0.01 M sodium phosphate (pH 6.8), 1 mM EDTA (pH 7.6), 0.5% SDS, 100 μg/ml denatured salmon sperm DNA and 0.1% nonfat dried milk, hybridization temperature of 2-2.5° C. below the T_(m), final wash solution of 3 M TMACI, 0.01 M sodium phosphate (pH 6.8), 1 mM EDTA (pH 7.6), 0.5% SDS at 1-1.5° C. below the T_(m), final wash solution of 6×SSC, and final wash at 22° C.; whereas mild hybridization is effected by a hybridization solution of 6×SSC and 1% SDS or 3 M TMACI, 0.01 M sodium phosphate (pH 6.8), 1 mM EDTA (pH 7.6), 0.5% SDS, 100 μg/ml denatured salmon sperm DNA and 0.1% nonfat dried milk, hybridization temperature of 37° C., final wash solution of 6×SSC and final wash at 22° C.

Once markers of genetic disorders are identified, the probes of the present invention can be employed to determine predisposition of a subject to a genetic disorder.

Diagnostic probes prepared according to the teachings of the present invention can be attached to a solid substrate, which may consist of a particulate solid phase such as nylon filters, glass slides or silicon chips [Schena et al. (1995) Science 270:467-470].

In a particular embodiment, oligonucleotide probes prepared according to the teachings of the present invention can be attached to a solid substrate configured as a microarray. Microarrays are known in the art and consist of a surface to which probes that correspond in sequence to gene products (e.g., cDNAs, mRNAs, cRNAs, polypeptides, and fragments thereof), can be specifically hybridized or bound at a known position (regiospecificity).

Several methods for attaching the oligonucleotides to a microarray are known in the art including but not limited to glass-printing, described generally by Schena et al., 1995, Science 270:467-47, photolithographic techniques [Fodor et al. (1991) Science 251:767-773], inkjet printing, masking and the like. Methods of fabricating protein arrays are disclosed in U.S. Pat. No. 6,406,840.

Recombinant polynucleotides and probes generated according to the teachings of the present invention can be included in diagnostic or therapeutic kits. For example, oligonucleotides sets pertaining to specific disease related genes can be packaged in a one or more containers with appropriate buffers and preservatives along with suitable instructions for use and used for diagnosis or for directing therapeutic treatment.

Preferably, the containers include a label. Suitable containers include, for example, bottles, vials, syringes, and test tubes. The containers may be formed from a variety of materials such as glass or plastic.

Additional objects, advantages, and novel features of the present invention will become apparent to one ordinarily skilled in the art upon examination of the following examples, which are not intended to be limiting. Additionally, each of the various embodiments and aspects of the present invention as delineated hereinabove and as claimed in the claims section below finds experimental support in the following examples.

EXAMPLES

Reference is now made to the following examples, which together with the above descriptions, illustrate the invention in a non limiting fashion.

Generally, the nomenclature used herein and the laboratory procedures utilized in the present invention include molecular, biochemical, microbiological and recombinant DNA techniques. Such techniques are thoroughly explained in the literature. See, for example, “Molecular Cloning: A laboratory Manual” Sambrook et al., (1989); “Current Protocols in Molecular Biology” Volumes I-III Ausubel, R. M., ed. (1994); Ausubel et al., “Current Protocols in Molecular Biology”, John Wiley and Sons, Baltimore, Md. (1989); Perbal, “A Practical Guide to Molecular Cloning”, John Wiley & Sons, New York (1988); Watson et al., “Recombinant DNA”, Scientific American Books, New York; Birren et al. (eds) “Genome Analysis: A Laboratory Manual Series”, Vols. 1-4, Cold Spring Harbor Laboratory Press, New York (1998); methodologies as set forth in U.S. Pat. Nos. 4,666,828; 4,683,202; 4,801,531; 5,192,659 and 5,272,057; “Cell Biology: A Laboratory Handbook”, Volumes I-III Cellis, J. E., ed. (1994); “Current Protocols in Immunology” Volumes I-III Coligan J. E., ed. (1994); Stites et al. (eds), “Basic and Clinical Immunology” (8th Edition), Appleton & Lange, Norwalk, Conn. (1994); Mishell and Shiigi (eds), “Selected Methods in Cellular Immunology”, W. H. Freeman and Co., New York (1980); available immunoassays are extensively described in the patent and scientific literature, see, for example, U.S. Pat. Nos. 3,791,932; 3,839,153; 3,850,752; 3,850,578; 3,853,987; 3,867,517; 3,879,262; 3,901,654; 3,935,074; 3,984,533; 3,996,345; 4,034,074; 4,098,876; 4,879,219; 5,011,771 and 5,281,521; “Oligonucleotide Synthesis” Gait, M. J., ed. (1984); “Nucleic Acid Hybridization” Hames, B. D., and Higgins S. J., eds. (1985); “Transcription and Translation” Hames, B. D., and Higgins S. J., Eds. (1984); “Animal Cell Culture” Freshney, R. I., ed. (1986); “Immobilized Cells and Enzymes” IRL Press, (1986); “A Practical Guide to Molecular Cloning” Perbal, B., (1984) and “Methods in Enzymology” Vol. 1-317, Academic Press; “PCR Protocols: A Guide To Methods And Applications”, Academic Press, San Diego, Calif. (1990); Marshak et al., “Strategies for Protein Purification and Characterization—A Laboratory Course Manual” CSHL Press (1996); all of which are incorporated by reference as if fully set forth herein. Other general references are provided throughout this document. The procedures therein are believed to be well known in the art and are provided for the convenience of the reader. All the information contained therein is incorporated herein by reference.

It is appreciated that certain features of the invention, which are, for clarity, described in the context of separate embodiments, may also be provided in combination in a single embodiment. Conversely, various features of the invention, which are, for brevity, described in the context of a single embodiment, may also be provided separately or in any suitable subcombination.

Example 1 Latent Splicing in CAD pre-mRNA is Activated by Point Mutating in-frame Stop Codons

The accuracy and efficiency of pre-mRNA splicing is multifactorial dependent, including trans-acting factors and cis-acting sequence elements. Currently known cis acting sequence elements include 5′ and 3′ splice sites, a branch point, a polypyrimidine tract and splicing enhancer and silencer sequence elements. A key step in pre-mRNA splicing involves the recognition and selection of a 5′SS consensus sequence such as the mammalian AG/GTRAGT sequence [SEQ ID NO: 1, where R denotes purine and “/” denotes the splice junction, Black (1995) RNA 1, 763-771; Kramer (1996) Annu. Rev. Biochem. 65, 367-409; Burge (1999) in The RNA World, second edition, eds. Gesteland, R. F., Cech, T. R. & Atkins, J. F. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y. pp. 525-560).

Frequently, sequences that comply with the consensus are not selected for splicing [Green (1991) Annu. Rev. Cell. Biol. 7:559-599]. Such 5′ consensus sequences are referred to as latent 5′SSs, splicing events in which such sites are utilized are referred to as ‘latent splicing’ and the resulting MRNA is referred to as latent RNA.

While reducing the present invention to practice the present inventors hypothesized that intronic stop codons located upstream to the latent site in the reading frame determined by the bona fide exons can silence splicing of the 5′SS.

To address this model, the in-frame intronic stop codons upstream of a 5′SS latent site in the multi-functional CAD (Carbamoyl-phosphate synthetase, Aspartate trans-carbamylase, Dihydroorotase, GenBank Accession No. M31621.1) gene were manipulated.

Experimental Procedures DNA and Plasmids

Ex1-Ex2 of the CAD constructs was derived from the CAD genomic plasmid p209 [Padgett, R. A., Wahl, G. M. & Stark, G. R. (1982) Mol. Cell. Biol. 2, 293-301], covering the 5′ end of the gene [Farnham, P. J. & Kollmar, R. (1990) Cell Growth Differ. 1, 179-189] and containing EcoRI and SalI restriction sites. ExN-ExN+3 was a SalI—PstI fragment from the CAD genomic plasmid pGS [Burge (1999) in The RNA World, second edition, eds. Gesteland, R. F., Cech, T. R. & Atkins, J. F. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y. pp. 525-560]. The Ex1-Ex2 fragment was inserted into the EcoRI—SalI site of pGS, and the EcoRI—Sphl fragment of this plasmid was cloned into the respective sites of pcDNAI/Amp.

The three fragments used to construct CAD mutants (i.e., Muts 1-4) by the Power-Cloning technology (Gesher Advanced Biotechs, Israel, WO98/38297, WO98/38298 and WO98/38299) were as follows: (i) A 5601-bp Bpu11021 fragment cut from CAD2 and purified by gel electrophoresis; (ii) A 135-bp PCR fragment which harbored the mutation(s) generated by the PCR primers listed in Table 1, hereinbelow (mutated nucleotides are underlined): TABLE 1 SEQ ID Primer Nucleotide Sequence NO: Mut1 Mut2 Mut3 Mut4 1 ATCAAGTGCACCAAACTCTTCGTGGAGGTGGCACAG 2 + + 2 ATCAAGTGCACCAAACTCTTCGTGGAGGTGGGACAG 3 + + 3 CACAAAGCTCCACCGCTAGCTCAGCCCTTATACG 4 + + 4 CACAAAGCTCCACCGCTAGCTGAGCCCTTATACG 5 + +

Primers 1 and 2 include sequences, which flank the Earl site, and primers 3 and 4 include sequences which flank the “right” Bpu11021 site;

-   -   (iii) A 572 bp PCR fragment that includes sequences flanking the         “left” Bpu11021 site at one end and sequences flanking the Earl         site at the other end. The fragment was prepared by PCR         amplification using the sense primer         5′-GCCTGCTCTCCAGCGCCCCGCTC-3′ (SEQ ID NO: 6) and the antisense         primer 5′-ACGAAGAGTTTGGTGCACTTGATG-3′ (SEQ ID NO: 7).

PCR fragments were purified by gel electrophoresis.

Mutant 5 was generated by inserting a 856 nt XmaI-Sphl fragment flanking the mutated downstream stop codon in Mut 1 into the respective site in the CAD2 construct. The remaining CAD mutant constructs were prepared by the QuickChange PCR-based mutagenesis method (Stratagene, Torrey Pines Road, La Jolla, Calif.).

For the frame-shift mutants, Mut 6 and Mut 7, the following primers were used to insert an AT dinucleotide (underlined) at a distance of 53 nt downstream of the normal 5′ splice site in CAD2 and Mut 2 to generate Mut 6 and Mut 7, respectively: sense primer 5′-GGGGGGATGAGCGTGCATGCTGGGGTTGGGAG-3′ (SEQ ID NO: 8) and antisense primer 5′-CTCCCAACCCCAGCATGCACGCTCATCCCCCC-3′ (SEQ ID NO: 9). The TGA located 32 nt further downstream was thus frame shifted, and no new in-frame stop codons were generated.

To mutate the downstream TGA stop codon (S86) in Mut 2 the following primer pairs were used (mutated nucleotides are underlined): Mut 10 (TGA: to TAG): Sense primer (SEQ ID NO: 10) 5′-GCAGCGTATAAGGGCTAGGCTAGCGGTGGAGCT-3′; and Antisense primer (SEQ ID NO: 11) 5′-AGCTCCACCGCTAGCCTAGCCCTTATACGCTGC-3′. Mut 11 (TGA to TAA): Sense primer (SEQ ID NO: 12) 5′-GCAGCGTATAAGGGCTAAGCTAGCGGTGGAGCT-3′; and Antisense primer (SEQ ID NO: 13) 5′-AGCTCCACCGCTAGCTTAGCCCTTATACGCTGC-3′. Mut 12 (TGA to TGG), Sense primer (SEQ ID NO: 14) 5′-GCAGCGTATAAGGGCTGGGCTAGCGGTGGAGCT-3′; and Antisense primer (SEQ ID NO: 15) 5′-AGCTCCACCGCTAGCCCAGCCCTTATACGCTGC-3′.

To generate Mut 9, in which all four stop codons in CAD1 were mutated in a single step, the sense primer 5′-CGGGTGCAGGAGTGTACAGCTGTGAAGGGGGGAAGAGCGTGCGCTGGGG TTG-3′ (SEQ ID NO: 16) and antisense primer 5′-CAACCCCAGCGCACGCTCTTCCCCCCTTCACAGCTGTACACTCCTGCACCC G-3′ (SEQ ID NO: 17), were used. S25 was mutated by a T insertion at position 27 (boldface), thereby frame shifting S34, S79, and S91 (see FIGS. 2 b and 5 a). This insertion also shifted the TGA triplet at position 45 into the reading frame. This stop codon was eliminated by a T to A mutation (underlined).

Transfections—Syrian hamster SV28 fibroblast cells and human 293T cells were grown to 50% confluence in tissue culture plates as described [Miriami, E., Sperling, J. and Sperling, R. (1994) Nucleic Acids Res. 22, 3084-3091], and transiently transfected with the indicated DNA constructs (10 μg or 2 μg per 5×10⁶ SV28 or 293T cells, respectively) using the calcium phosphate method [Kingston (1992) in Short protocols in molecular biology, eds. Ausubel, F. M., Brent, R., Kingston, R. E., Moore, D. D., Seidman, J. G., Smith, J. A. & Struhl, K. (John Wiley and Sons, NewYork), pp. 9.1-9.16]. Cells were harvested 24 or 48 hours following transfection and total cellular RNA was extracted with guanidinium thiocyanate as described [Miriami, E., Sperling, J. and Sperling, R. (1994) Nucleic Acids Res. 22, 3084-3091].

RT-PCR—Total RNA was treated with RNase-free DNase I (50 U/ml; Promega), and cDNA was synthesized from 1 μg of RNA with dT₁₅ primer using MMLV reverse transcriptase (Gibco BRL, Crewe UK). PCR reactions (20 μl) contained cDNA synthesized from 0.2 μg of total RNA, 10 pmole of each of the indicated primer pairs (listed in Table 2 hereinbelow), and 1.0 units of Taq DNA polymerase (Roche Molecular Diagnostics, Pleasanton Calif. USA). Amplification was carried out in a DNA Programmable Thermal Controller (PTC-100; MJ Research, Inc.) for 30 cycles, at annealing temperature of 63° C. (for primer pairs a+b) or 58° C. (for primer pair c+b). The amplified products were analyzed by electrophoresis in 2% agarose gels. The identity of the bands was confirmed by sequencing of the DNA extracted from a gel and purified with a commercial DNA purification kit (QIAGEN, Chatsworth, Calif. USA). TABLE 2 Primer identity Primer Sequence SEQ ID NO: a sense CTCAGATCCTGGTCGACGGC 18 a′ sense CTCAGATCCTGGGTCGACGGC 19 b antisense CAGGGAGCCGCACCAGTTTC 20 c sense CCGGGTGCAGGAGTGACAGC 21 c′ sense CCGGGTGCAGGAGTGTACAGC 22 Note that primers a′ and c′ were used to amplify Mut 9.

For PCR analysis of β-globin RNA the following primers from exon 1 were used; Sense: 5′ CCTGAAGTTCTCAGGATCC 3′ (SEQ ID NO: 23). Antisense: 5′ AGGAGAAGTCTGCCGTTAC 3′ (SEQ ID NO: 24).

Quantitative PCR—To ensure that PCR was performed under linear conditions, the following quantitative PCR protocol was used. For each transfection, cDNAs were synthesized from 1 μg, 0.33 μg, 0.1 μg, and 0.033 μg of total RNA. PCR amplification was performed with primer pair a+b using the reaction conditions as above. Amplification was carried out for 15, 20, 25 and 30 cycles, and the DNA from each reaction was analyzed by Southern blot hybridization using ³²P-labeled Primer 6. The autoradiograms were quantified with MacBas 2.5 software.

S1 Nuclease Mapping—To verify the RT-PCR results, the RNAs expressed from CAD2, Mut 1, and Mut 2 constructs were analyzed by the independent S1 nuclease mapping method using a 3′ end labeled 951-bp BsrFI fragment from CAD2. S1 nuclease mapping was carried out essentially as previously described [Miriami, E., Sperling, J. & Sperling, R. (1994) Nucleic Acids Res. 22, 3084-3091]. Probe labeling was effected by gel purifying the 951-bp BsrFI fragment from CAD2 and 3′ end labeling with [α-³²P]dCTP and [α-³²P]dGTP using the Klenow fragment of DNA polymerase I.

Results

Latent splicing in CAD pre-mRNA is activated upon removal of in-frame stop codons—The wild type CAD chimeric mini gene containing the first two exons and the first intron of the CAD gene (Ex1-Ex2) fused in-frame to a downstream CAD subgenomic region composed of four exons and three introns (ExN-ExN+3) was inserted into pcDNAI/Amp expression vector (Invitrogen, The Netherlands). Two constructs, designated CAD1 and CAD2, were cloned. DNA sequencing confirmed an open reading frame in ExN of CAD1, and revealed four in-frame stop codons between the normal and the latent 5′SSs in the downstream intron (IntN). CAD2 included a single nucleotide deletion in the Ex2-ExN junction. DNA sequencing confirmed that ExN in this construct maintained an open reading frame, and revealed two in-frame stop codons in the same region of IntN (FIG. 2 a).

The indicated mini gene constructs were transfected into Syrian hamster or 293T cells and the transiently expressed CAD RNAs were analyzed by RT-PCR.

FIG. 2 b shows the amplified PCR fragments produced from primer a (see Table 2), which spans the junction between exon 2 and exon N and primer b (see Table 2), which is complementary to a sequence within the downstream exon N+1.

Analysis of RNA from control untransfected cells, showed that endogenous CAD RNA was not amplified (FIG. 2 b, lane 2). Transfection with a wild type CAD mini gene construct (i.e., CAD1), which contained four in-frame stop codons upstream of the latent site in intron N (FIG. 2 a, upper scheme), gave rise to a 428-base pair (bp) DNA fragment representing the pre-mRNA and/or remnants of the mini gene DNA and a 203-bp fragment representing normally spliced CAD RNA (normal RNA, FIG. 2 b, lane 3). CAD2, which contained two in-frame stop codons upstream of the latent site in intron N (FIG. 2 a, lower scheme), gave similar results (FIG. 2 b, lane 4). Notably, neither constructs gave rise to latent splicing. However, as predicted, elimination of all stop codons from both CAD1 and CAD2, allowed latent splicing in the respective mutants.

Thus, a construct in which both stop codons in CAD2 were mutated [S2: TGA to TGG, S86: TGA to TCA, Mut 1; FIG. 2 b, lane 5] gave rise to a fragment of 328 bp which corresponded to an RNA species produced by a splicing event at the latent 5′SS. Mutating the upstream stop codon (S2) in CAD2, which is located within the normal 5′SS, increased the number of mismatches with the consensus at this site from two to three. However, the alteration in the splicing pattern could not be attributed to this change, since a construct in which both stop codons were mutated, but the normal 5′SS was strengthened by an additional C to G mutation, restoring the number of mismatches with the consensus to two (Mut 3; FIG. 2 b, lane 7), gave rise to splicing at both the normal and latent sites. For control, a double mutation in the normal 5′SS alone was used. Such a construct which did not seem to perturb splicing from the normal splice site, was not sufficient to elicit latent splicing (Mut 4; FIG. 2 b, lane 8). Furthermore, a construct in which only the stop codon included in the normal 5′SS (S2) was mutated, leaving the downstream stop codon (S86) unchanged, did not give rise to latent RNA but normal splicing was observed (Mut 2; FIG. 2 b, lane 6).

To exclude the possibility that latent splicing occurs in transcripts containing in-frame stop codons, but amplification thereof by PCR is suppressed by the high concentration of normally spliced RNA [Valentine (1997) RNA 3, 660-676], PCR amplification was performed using the intronic primer (Table 2, primer c) and primer b (Table 2, FIG. 2 c). These primers were not expected to amplify the normally spliced RNA, so that suppression of amplification of the latent RNA was not expected to take place. However as shown in FIG. 2 c, no PCR product arising from the latent RNA was observed in cells expressing the wild type constructs (FIG. 2 c, lanes 3, 4), or in cells expressing constructs in which only S2 was mutated to a sense codon (FIG. 2 c, lanes 6, 8). Mutating both stop codons to sense codons, however, gave rise to the latent RNA (FIG. 2 c, lanes 5, 7), thereby substantiating the results shown in FIG. 2 b.

To further demonstrate the null phenotype of latent splicing in stop-codon-containing constructs, quantitative RT-PCR analysis under linear conditions was employed. For each transfection, cDNAs were synthesized from 1 μg, 0.33 μg, 0.1 μg, and 0.033 μg of total RNA. PCR amplification was performed with primer pair a+b using the reaction conditions as above. Amplification was carried out for 15, 20, 25 and 30 cycles, and the DNA from each reaction was analyzed by Southern blot hybridization using ³²P-labeled antisense primer (SEQ ID NO: 7). Thus, 30 fold serial dilutions of input RNA and 15 to 30 cycles of amplification displaying total amplification range of more than four orders of magnitude, assuming an average amplification of 1.5-fold per cycle, revealed latent splicing only in mutants lacking stop codons but not in WT or mutants containing stop codons (data not shown). Thus, latent nonsense RNA in quantities larger than 0.0076% of normally spliced RNA should have been detected by this analysis.

The RT-PCR results were confirmed by S1 nuclease mapping. FIG. 7 b shows that splicing at the latent 5′ splice site occurred only in cells expressing the double mutant construct (Mut 1, FIG. 7 b lane 3) but not in cells expressing CAD2 (FIG. 7 b lane 2) or Mut 2 (FIG. 7 b lane 4). FIG. 3 c confirms this result by showing that the 294 bp fragment, which represents splicing at the latent 5′ splice site, could not be observed in Mut 2 RNA even when the highest concentration of input RNA was used (FIG. 7 b lane 7). In comparison, the 294 bp fragment was detected already in the lowest amount of Mut 1 RNA (FIG. 7 b lane 2). These results suggest that activation of splicing at an intronic latent 5′ splice site occur upon elimination of upstream in-frame stop codons.

Example 2 Activation of Latent Splicing Cannot be Attributed to Interference with Splicing Control Elements

The relative efficiencies of alternative splicing events may often be influenced by short enhancer sequences [Liu (2000) Mol. Cell. Biol. 20:1063-1071; Schaal (1999) Mol. Cell Biol. 19:261-273], as well as other splicing control elements that suppress or enhance splicing [Black (1995) RNA 1:763-771; Berget (1995) J. Biol. Chem. 270:2411-2414; Blencowe (2000) Trends. Biochem. Sci. 25:106-110; Wang (1997) Curr. Opin. Genet. Dev. 7:205-211]. The possibility that activation of latent splicing can be attributed to suppression of a splicing silencing element or to activation of a splicing enhancing element, was therefore addressed

Results

As shown in FIGS. 3 a-b mutating either S2 (i.e., Mut2) or S86 (i.e., Mut5) alone did not give rise to latent splicing (Mut 2 and Mut 5; FIGS. 3 a-b, lanes 3 and 4, respectively), while latent splicing was elicited only when both S2 and S86 were mutated (Mut 1; FIGS. 3 a-b, lane 2). Furthermore, latent splicing was suppressed when the TGA stop codon in S86 of Mut 2 was mutated to either of the remaining stop codons TAG or TAA (Mut 10 and Mut 11; FIGS. 3 a-b, lanes 5 and 6, respectively), while mutating S86 to the missense codon TGG elicited latent splicing (Mut 12; FIGS. 3 a-b, lane 7).

Thus, the phenotypic behavior of mutants 10-12 supported the conclusion that the effect on latent splicing should be attributed to the reading context of the mutation in S86 rather than the mutation per se.

However, since splicing enhancer and silencer sequence elements are degenerate and location thereof is not precisely defined with respect to the splice junctions [Blencowe (2000) Trends Biochem. Sci. 25:106-110; Liu (2001) Nat. Genet. 27:55-58], frame shift mutation analysis was effected. A dinucleotide AT was inserted 53 nt downstream of the normal 5′SS, thereby frame shifting the S86 TGA located 33 nt further downstream. Frame shifting of S86 alone, leaving S2 unchanged, did not give rise to latent RNA but gave rise to normal RNA (Mut 6; FIGS. 4 a-b, lane 3). On the other hand, a frame shift mutation of S86 together with a point mutation in S2 resulted in latent splicing (Mut 7; FIGS. 4 a-b, lane 4). Likewise, a frame shift mutation in CAD1, eliminating all four stop codons upstream of the latent site, also gave rise to latent splicing (Mut 9; FIGS. 4 a-b, lane 5). These results substantiate the significance of the reading context of putative stop codons, rather than the sequence in which they are embedded, in rendering a downstream 5′SS latent.

Example 3 Suppression of Latent Splicing is not Alleviated by Drugs that Abrogate Nonsense-Mediated mRNA Decay (NMD)

Messenger RNAs which contain premature translation termination codons (PTCs) lead to truncated proteins, which can be toxic to cells if they function in a dominant-negative or gain-of-function fashion [Li (1998) Immunity 8, 135-141; Hentze (1999) Cell 96, 307-310; Frischmeyer (1999) Hum. Mol. Genet. 8, 1893-1900.]. Numerous studies have shown that the nuclear and cytoplasmic abundance of many nonsense mRNAs expressed in mammalian cells is reduced. This was attributed to NMD, whereby the occurrence of PTCs activates a mechanism which rapidly degrades such aberrant mRNAs (Li Supra; Hentze Supra; Frischmeyer Supra; Maquat (1995) RNA 1:453-465].

In the reported cases of NMD, the levels of nonsense mRNAs were substantially reduced but remained detectable [1-30% of the normal message (Li Supra; Maquat Supra]. Interestingly, no PTC-containing CAD RNA was detected in cells expressing constructs harboring intronic in-frame stop codons upstream of the latent 5′SS, whether analyzed by RT-PCR or nuclease S1 mapping.

To exclude the possibility that latent splicing had occurred, but the resulting nonsense RNAs were subjected to rapid degradation by NMD to an extent that rendered them undetectable, the splicing pattern of CAD RNAs, expressed from several constructs, in cells treated with drugs [e.g., Cycloheximide (CHX), aminoglycoside antibiotic G-418] known to abrogate NMD was tested. Other protein synthesis inhibitors shown to efficiently reverse the down regulatory effects of PTCs in exons of the T-cell receptor-β and the β-globin mRNAs [Carter (1995) J. Biol. Chem. 270:28995-29003] and in the HEXA mRNA [Rajavel (2001) Mol. Cell Biol. 21:5512-5519] were tested as well.

Results

FIGS. 5 a-b show that treatment with CHX does not alter CAD splicing patterns. Notably, latent splicing was not detected in cells expressing constructs including in-frame stop codons upstream of the latent 5′SS including CAD1 having four stop codons (FIG. 5 a, lanes 1-4), CAD2 including two stop codons (FIG. 5 a, lanes 5-7), Mut 2 having one stop codon (FIG. 5 a, lanes 8-10), in the presence or absence of CHX. Latent splicing was, however, observed only when stop codons were absent (Mut 1) and was not affected by CHX (FIG. 5 a, lanes 11-13).

The CHX experiments were performed under conditions in which NMD was eliminated in 293T cells, as shown in FIG. 5 b. For this experiment 293T cells were co-transfected either with a wild type β-globin construct (WT, FIG. 5 b, lanes 1-3), or with a PTC-containing β-globin construct (Ter 39) together with CAD1 as a control (FIG. 5 b, lanes 4-6). FIG. 5 b (lanes 1-3) shows that the expression of WT β-globin RNA did not change upon CHX treatment. However, the level of Ter 39 β-globin RNA was reduced significantly (FIG. 5 b, lane 4), presumably due to NMD, and treatment with CHX reversed this effect (FIG. 5 b, lanes 5 and 6).

To further exclude the possibility that an unusual rapid degradation by NMD may have accounted for the absence of transcripts spliced at the latent 5′SS in wild type CAD RNA, CAD RNA that contains a PTC in a bona fide exon (CAD Ter) was analyzed. If this interpretation were valid, the transcript expressed from CAD Ter should be undetectable as well. In contrast, FIG. 5 b (lane 7, upper panel) shows that CAD Ter RNA was detected. Furthermore, the stability of this nonsense RNA increased by about 40% upon treatment with CHX (FIG. 5 b, lanes 8 and 9, lower panel), as estimated by comparing to the co-expressed GFP RNA reference (lower panel).

Taken together, these results suggest that the absence of a signal for nonsense RNA should be attributed to the suppression of the latent 5′SS by the presence of upstream in-frame stop codons.

Example 4 Latent Splicing is Activated in the α-L-Iduronidase (IDUA) Gene by Mutating an in-frame Stop Codon Upstream of the Latent 5′ Splice Site

To generalize the role of in-frame intronic stop codons in latent splicing, RNA expressed from the human IDUA gene was analyzed [Neufeld (1991) Ann. Rev. Biochem. 60:257-280]. Sequence examination of this gene [Scott (1992) Genomics 13:1311-1313] revealed a latent site within the first intron, which is preceded by an in-frame stop codon (FIG. 6 a). The effect of missense mutating this stop codon on latent splicing was addressed.

Experimental procedures

DNA and Plasmids

A plasmid carrying a 9 kb fragment from the 5′ end of the IDUA gene [Bach (1993) Am. J. Hum. Genet. 53:330-338], was provided by Dr. Elizabeth Neufeld, Department of Biological Chemistry, UCLA. The wild type IDUA mini-gene was constructed by cloning an 893-bp PCR fragment comprising the first IDUA intron flanked by the first two exons into pcDNAI/Amp expression vector (Invitrogen, The Netherlands). Mutant IDUA mini genes were prepared by the Power-Cloning technology as described in Example 1, hereinabove. Cloning was confirmed by DNA sequence analyses.

A normal β-globin construct (pmCMV-Gl-Normal) and a construct expressing a PTC-containing β-globin mRNA [pmCMV-Gl-39Ter Zhang (1998) RNA 4:801-815] were provided by Dr. L. E. Maquat University of Rochester, Rochester, N.Y.

RT-PCR

IDUA cDNA was generated using a primer that is complementary to the fusion region of IDUA with the pcDNAI/Amp vector (5′-AGAGGGCCCTCTAGATGCATG CTGGTGGTGACAAGCTCCAGCAGC-3′, SEQ ID NO: 25). The following primers were used for PCR: sense primer b 5′-CGAGCACGCGTGGCCATGCGT-3′ (SEQ ID NO: 26); antisense primer c 5′-AGGACGTACTGGTCAGCCTGG-3′ (SEQ ID NO: 27); sense primer d[+]5′-ACTGTGAGAGCTTCAGAGACC-3′ (SEQ ID NO: 28).

Analysis of IDUA RNA was carried out on total RNA, prepared 48 hr after transfection, by RT-PCR. For the preparation of IDUA cDNA a primer complementary to the fusion region of IDUA with the vector was used. PCR was effected as described for CAD (see Example 1) but with the addition of 5% DMSO, at an annealing temperature of 63° C. (primers b+c) or 59° C. (primers d+c).

Results

Chinese hamster ovary cells were transiently transfected with the wild type and mutant IDUA mini-genes, and the IDUA RNAs were analyzed by RT-PCR. As shown in FIGS. 6 a-c, total RNA from control untransfected cells gave no PCR signal corresponding to JDUA RNA with either combination of primers (FIG. 6 b and c, lane 2). PCR amplification with primers b and c of the RNA obtained from cells transfected with the wild type construct gave rise to the expected fragments representing IDUA pre-mRNA and normally spliced RNA (778 and 212 bp, respectively; FIG. 6 b lane 3). Amplification of the same RNA with primers d and c gave rise only to a PCR product of 537 bp representing the pre-mRNA (FIG. 6 c lane 3). Amplification with primers b and c of total RNA from cells transfected with the Mut 1 construct (FIG. 6 b lane 6) gave rise to the expected 778 bp pre-mRNA PCR product and to a 447-bp PCR product representing latent RNA. This result was confirmed by the nested PCR experiment (FIG. 6 c, lane 6), showing PCR products of 537 and 206 bp, representing the pre-mRNA and latent RNA, respectively.

Notably, the 212 bp fragment, which represents normally spliced IDUA RNA, was not detected in the Mut 1 IDUA RNA (FIG. 6 b, lane 6), though trace amounts of this band were detected by radioactive PCR (not shown), suggesting that the TGA to TGG mutation in Mut 1 rendered the normal 5′SS almost inactive in splicing. This observation was attributed to the fact that the number of mismatches with the consensus of the normal 5′SS increased from two in the wild type to three in the mutant. Therefore analogous experiments with constructs in which further mutations that decreased the number of mismatches with the consensus were introduced (Mut 2, two mismatches; Mut 3, one mismatch) were effected. FIG. 6 b (lanes 4, 5) shows that each one of these mutants gave rise to PCR products resulting from splicing at the normal 5′SS without impairing splicing from the latent 5′SS.

Finally, as observed in the CAD case, the null phenotype of latent splicing in IDUA gene constructs having an in-frame stop codon upstream of the latent 5′SS was maintained even after treatment with CHX and G-418 (not shown). Thus, it may be concluded that the absence of a signal for nonsense RNA should be attributed to the suppression of the latent 5′SS by the presence of upstream in-frame stop codons.

The identification of upstream in-frame stop codons, which activates latent splicing implies the existence of a nuclear surveillance mechanism that is functionally coupled to the splicing machine. By scanning the pre-mRNA, this mechanism detects the presence of in-frame stop codons and suppresses splicing at downstream potential 5′SSs, which could have led to the inclusion of PTCs in the mRNA. The hereinabove described results are consistent with studies that suggested a nuclear scanning mechanism. These include mutations in the DHFR gene [Urlaub (1989) Mol. Cell. Biol. 9:2868-2880] and several cases of human genetic diseases in which exons harboring PTCs were skipped (Bach Supra; Maquat (1995) Supra; Dietz (1993) Science 259:680-683; Dietz (1994) Nat. Genet. 8:183-188]. In the fibrillin gene, associated with Marfan syndrome, nonsense, but not missense, mutations were associated with skipping of exon 51 Dietz (1994) Supra]. These studies also include cases of intron retention [Naeger (1992) Genes Dev. 6:1107-1119; Lozano (1994) EMBO J. 13:4617-4622; Aoufouchi (1996) Cell 85:415-422; Gersappe (1999) J. Biol. Chem. 274:22452-22458; Muhlemann (2001) Mol. Cell 8:33-44]. In particular, nonsense mutations in the Igβ gene cause defective splicing of this pre-mRNA in a B cell in vitro system [Aoufouchi supra]. While the above studies dealt with the effect of mutations which generate exonic in-frame stop codons, the present study addresses the issue of nonsense RNA from the viewpoint of splice site selection and the role endogenous intronic stop codons play in this process.

The observation that a large number of protein-coding transcripts that contain nonsense mutations in their exons are spliced, despite the above-described is highly significant since such nonsense transcripts are characteristic of many genetic diseases [Culbertson (1999) Trends Genet. 15:74-80]. A clue to a possible answer lies in the sequence environment in which the stop codons are embedded. In the hereinabove described, the intronic in-frame stop codons are flanked by 5′SSs on both sides. In the absence of stop codons, two alternative exons can be defined by the exon definition process [Berget (1995) J. Biol. Chem. 270:2411-2414] and independently, or in a regulated fashion, enter the splicing pathway. The presence of an in-frame stop codon between the alternative 5′SSs apparently interferes with the exon definition involving the downstream one, thereby suppressing participation thereof in splicing. A different situation arises when a stop codon is located in a bona fide exon, where it is flanked by an upstream 3′SS and a downstream 5′SS, as is the case for most nonsense transcripts that are spliced and contain PTCs in their exons. It is possible that interference with the exon definition process has the alternative of choosing a further downstream 3′SS, thereby skipping the PTC-containing exon, alternatively it may result in intron retention. However, if no alternative splice choices that could eliminate the in-frame stop codon are available, such “ill-defined exons” might escape the surveillance mechanism and enter the splicing pathway. This would result in the production of PTC-containing mRNAs that can be subjected to the NMD pathway.

Such a surveillance mechanism is difficult to conceive mainly because it implies that the reading frame of mRNAs can be recognized at the level of pre-mRNA before splicing commences. The machine performing this role could involve intranuclear ribosomes. Support for such a view is the occurrence in the nucleus of charging of tRNA [Lund (1998) Science 282:2082-2085], translation initiation factors [Dostie (2000) J. Cell Biol. 148:239-247], and coupled transcription and translation [Iborra (2001) 293:1139-1142]. Alternatively, a yet unknown nuclear machine might perform this reading frame task. But even if a nuclear ‘ribosome-like’ machine, capable of reading nucleotide triplets was invoked [Li (1998) Supra; Frischmeyer (1999) Supra], it would be difficult to envisage its function on a pre-mRNA because the presence of introns whose length is not an integer multiple of three alter the reading frame. However, a supraspliceosome complex which serves as a frame onto which the pre-mRNA is folded to align exons about to be spliced, while introns are looped out of each of the respective spliceosomes [see FIG. 5 in Muller (1998) J. Mol. Biol. 283:383-394], allows exon sequences to be scanned consecutively even when introns are still part of the pre-mRNA, suggesting that the decision whether to splice or not is made at the level of the complex. Namely, splicing complexes in which a latent 5′SS is aligned with a 3′SS may be formed, but splicing does not take place because an in-frame stop codon is recognized upstream of that site in the context of the reading frame of the not-yet-formed mRNA. Such unproductive complexes may reassociate to form productive splicing complexes. When the stop codon is removed, the homologous complex is stable and is capable of entering the splicing pathway.

In summary, the suppression of splicing (SOS) mechanism proposed here acts to prevent the inclusion of PTCs in mRNAs rather than dealing with them after splicing by activating NMD. Despite this conceptual difference between NMD and SOS, it is plausible that independent or complementary nuclear and cytoplasmic mechanisms are required to alleviate the potentially toxic effect of in-frame stop codons.

Example 5 A Computerized Survey for Latent 5′ Splice Sites in 446 Protein-Coding Human Genes Experimental Procedures

Database—The data were derived from a non-redundant complete human gene sequences data base (http://www.fruitfly.org/seq_toools/datasets/Human/coding_data/). The data were further filtered and 16 genes were excluded based on the criteria that they were described as pseudogenes or partial [Burge (1999) in The RNA World, second edition, eds. Gesteland, R. F., Cech, T. R. & Atkins, J. F. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y. pp. 525-560]. After this filtering, the data set included 446 spliced genes.

Identification of 5′ splice site signals—A program in C language was written to search for 5′ splice site signals within the database. The criteria for the search for 5′ splice site consensus sequences are detailed in the Results. Intronic in-frame stop codons refer to the reading frame of the preceding exon.

The identified 5′ splice site consensus sequences were represented as weight matrices and presented in a logo representation produced by the PICTOGRAM program [http://genes.mit.edu/pictogram.html Lim and Burge supra]. The representation of signals as a weight matrix allows also for the evaluation of its degree of conservation by computing information content thereof.

Results

As described hereinabove splicing at latent 5′ splice sites could be activated upon removal of in-frame stop codons that are located between the normal and the latent sites [Li (2002) Proc. Natl. Acad. Sci. USA 99:5277-5282, FIGS. 8 a-b). This finding provided an experimental proof to the hypothesis that intronic in-frame stop codons play a role in the maintenance of an open reading frame in mRNAs by rendering downstream 5′ splice sites as latent.

To generalize this hypothesis, the frequency of 5′ splice site consensus sequences in protein-coding pre-mRNAs was addressed. Thus, a computer search for 5′ splice site consensus sequences within a non-redundant complete human gene sequences from the GenBank was performed. This data set includes 446 multi-exon genes having a total of 2,311 introns. The search algorithm allowed for a maximum of two mismatches in the consensus octanucleotide AG/GTRAGT (SEQ ID NO: 29), excluding the dinucleotide GT (underlined), which invariably appears at the 5′ end of U2 introns [Burge supra; Mount (1982) Nucleic Acids Research 10:459-472; Ohshima (1987) J. Mol. Biol. 195:247-259; Shapiro (1987) Nucleic Acids Research 15:7155-7174]. The use of this criterion is justified because 85.5% of the normal 5′ splice sites in this data set deviate from the consensus by no more than two nucleotides, thereby allowing each of most of the latent 5′ splice sites to compete with the respective normal 5′ splice site for a downstream 3′ splice site. Of the 2,311 normal 5′ splice sites, a total of 1,977 sites were picked up by this search. The remaining 334 normal 5′ splice sites deviate from the consensus by three (305) or more (29) mismatches. As shown in Table 3, below, in addition to these 2,311 normal 5′ splice sites, the search revealed 10,626 intronic 5′ splice sites consensus sequences which are located within 1,601 introns, whereas 710 introns are devoid of internal 5′ splice sites consensus sequences. It should be pointed out, that 5′ splice site consensus sequences are significantly less abundant in exon sequences, as only 551 were scored in 429 of the 2,311 exons. TABLE 3 Occurrence of 5 ′SS consensus sequences in 446 human genes Number of Sequences Sequences with consensus without Total consensus 5′ SS^(b) 5′ SS^(a) consensus 5′ SS^(c) Introns 2,311 1,601 10,626 710 Exons  2,311^(d) 429 551 1,882 ^(a)Consensus 5′ SSs, excluding the normal 5′ SSs. ^(b)Number of introns or exons that contain at least one consensus 5′ SS. ^(c)Number of introns or exons that do not contain consensus 5′ SS. ^(d)Last exons were excluded from this count.

As shown in FIGS. 9 a-c introns having internal 5′ splice site consensus sequences do not differ from introns lacking such sites with respect to the weight matrices of their normal 5′ splice sites (FIGS. 9 a-b). To ascertain that these two matrices are not different, a χ² test to compare the nucleotide distributions throughout the aligned positions was applied. The null hypothesis that these two weight matrices are different was rejected (p<0.005). A χ² test to compare these two weight matrices and the weight matrix of the internal 5′ splice site sequences (FIG. 9 c) revealed that the nucleotide distributions throughout the aligned positions were not different, except at position +3 which exhibited a preference to G at the latent sites. Interestingly introns having internal 5′ splice site consensus sequences do not differ from introns lacking such sites with respect to their phases (zero, one, or two, according to whether the first nucleotide in the given intron is the first, second or third in a coding triplet, respectively). Similarly to previous analysis [Tomita (1996) Mol. Biol. Evol. 13:1219-1223], introns from both groups were shown to have a preference to phase zero as shown in Table 4 below, whereas introns of phase two are less abundant. However, the introns with and without internal 5′ splice site consensus sequences vary significantly with respect to the presence of stop codons, as described below. TABLE 4 Percentage of intron phases Phase Number of introns zero one two With consensus 5′ SS 1,601 44.72 36.67 18.61 Without consensus 5′ SS 710 46.62 35.35 18.03

To consider the possibility that the occurrence of in-frame stop codons upstream of internal 5′ splice site consensus sequences is a significant general phenomenon, which may be involved in the prevention of splicing at such sites, the occurrences of in-frame stop codons upstream to all internal 5′ splice site consensus sequences was scored (Table 5). Splicing at 136 internal 5′ splice site consensus sequences lacking upstream in-frame stop codons, which are located in 105 introns, would not change the reading frame of the resulting mRNAs. These sites are thus potential candidates for alternative splicing, and have therefore been excluded from the statistical analysis described below. The remaining 1,496 introns contain 10,490 latent 5′ splice sites—10,045 of which (95.8%) have at least one upstream in-frame stop codon. TABLE 5 Occurrence of in-frame stop codons upstream of intronic 5′ SS consensus sequences in 446 human genes Number of Number of introns 5′ SS Introns with stop codons 1,359^(a) 10,045^(b) Introns without stop codons   137^(c)   445^(d) Total introns with latent 5′ SSs 1,496 10,490 Introns with potential alternative 5′ SSs   105   136 Total 1,601 10,626 ^(a)Introns with in-frame stop codon upstream of the most 3′ latent site. ^(b)Latent 5′ SSs with upstream in-frame stop codons. ^(c)Introns without in-frame stop codon upstream of the most 3′ latent site. ^(d)Latent 5′ SSs without upstream in-frame stop codons.

The possibility whether in introns having latent 5′ splice sites, stop codons upstream of the latent sites occur more frequently than in introns lacking such sites, was addressed. A total of 1496 introns (of different lengths) that have latent 5′ splice sites and 710 introns that do not were examined. If N is the length of an intron in nucleotides, its effective number of codons (L) is the integral part of N/3, (N−2)/3 or (N−1)/3 (according to the reading phase being zero, one or two, respectively). The number of in-frame stop codons in each intron of effective length L was scored, and their density was calculated. Then, estimates and standard errors of the density of stop codons were calculated for each group using ratio estimate techniques [Cochran (1953) Sampling Techniques Wiley, New York]. For introns having latent 5′ splice sites, the estimate of the density of stop codons was 0.04840±0.00064 stop codons per effective number of codons, whereas for introns that do not have latent 5′ splice sites, the estimate of the density was only 0.03382±0.00110. This difference is highly significant (P<0.001). If, for introns having latent 5′ splice sites, only the upstream part (up to the most 3′ latent site) is considered, the estimate of the density is 0.04883±0.00069, which makes the difference between the two types of introns even more pronounced.

A slightly different approach is to consider whether or not each intron has any stop codons at all. If stop codons are distributed independently, the probability that an intron, whose effective number of codons is L, will not have any stop codons is a negative exponential function e^(−βL). For any given L, the probability of not having any stop codons is smaller, the larger β is. Out of 1496 introns that have latent 5′ splice sites, 137 do not have any stop codons upstream of the most 3′ latent site (Table 5); and out of 710 introns that do not have latent 5′ splice sites, 167 introns do not have any stop codons. From the data, maximum likelihood estimates (MLE) of β was derived. For introns having latent 5′ splice sites, the MLE of β was 0.04485±0.00007 (estimate±standard error), compared to only 0.03019±0.00006 for introns without latent 5′ splice sites. This difference is highly significant (P<0.001).

Conclusions

In a survey of a database consisting of 446 human protein-coding-genes 10,490 latent 5′ splice sites which are located within 1,496 introns were identified. The high abundance of latent 5′ splice sites in the genome indicates that the splicing machine must frequently and efficiently discriminate between normal 5′ splice sites and latent ones, and emphasizes the necessity for a mechanism that identifies such latent sites and renders them as latent. A suggested mechanism is provided in Example 4, hereinabove and in [Miriami et al. J. Struct. Biol. 140 (2002) 116-122].

Interestingly, of the 10,490 latent 5′ splice sites scored hereinabove, 10,045 (95.8%) have at least one in-frame stop codon in the upstream intronic sequence. Subsequent statistical analyses of the data confirmed that in-frame stop codons are significantly over represented in introns that harbor latent 5′ splice sites, in comparison to introns that lack such sites. Thus, a functional linkage between 5′ splice site selection and the necessity to maintain an open reading frame in the MRNA is strongly implicated. Further, because the occurrence of intronic latent 5′ splice sites, having upstream in-frame stop codons, appears to be widespread in the genome, a general mechanism is suggested. The suggested role of such mechanism is to identify in-frame stop codons and suppress splicing at latent downstream 5′ splice sites so that the deleterious effects of including PTCs in apparently wild type transcripts is avoided. Such a mechanism is referred to as suppression of splicing (SOS). Clearly, not all parameters that control splice site selection are known, and the relative importance of those that have already been characterized cannot be assessed as yet. Nonetheless, the relevance of the SOS mechanism for accurate gene expression is highlighted by the fact that 413 genes out of the 446 genes in the data base examined here have at least one intron with latent 5′ splice sites. Of these 413 genes, 404 (98%) have at least one intron with a latent 5′ splice site whose usage for splicing would introduce an in-frame stop codon into the resultant mRNA.

Example 6 Alternative Splicing of HTH can be Regulated by SOS

The hereinabove described computational analysis and mutational experiments suggested a functional linkage between 5′ splice site selection and the necessity to maintain an open reading frame in the mRNA. It was therefore suggested that such a linkage is mediated by a general mechanism termed suppression of splicing (SOS). To further substantiate this mechanism, in-frame stop codons were introduced in between two adjacent alternative 5′SS which are normally used to express splice variants of the human tyrosine hydroxylase (HTH, GenBank Accession No. D00269.1) gene [Dumas (1996) J. Neurochem. 67:19-25; Grima (1987) Nature 326:707-711] and the effect of such mutations on repression of splicing was thereafter determined.

Experimental Procedures

Plasmids—Wild type HTH-a construct containing the first three exons and two introns of HTH cloned into pcDNA3/Amp was provided by Dr. Jacques Mallet, Salpêtrièr Hospital, Paris. The mutant HTH mini genes were prepared by the Power-Cloning technology described in Example 1. HTH primer 1: [+] 5′-TAC GAC TCA CTA TAG GGA GAC CCA AGC T-3′ (SEQ ID NO: 32) and HTH primer 2: [−] 5′-CCT GGG CTC CGG TCC ACT GCG GCC GCC GGGCAC CTA CCT ACC CTC TTA CC-3′ (SEQ ID NO:33) were used to prepare HTH Mutl. HTH primer 1 and HTH primer 3: [−] 5′-CCT GGG CTC CGG TCC ACT GCG GCC GCC GGGCAC CTA CCT CCC CTC TTA CC-3′ (SEQ ID NO: 34) were used to generate hTH Mut2. The incorporation of the appropriate mutations and the preservation of the reading frame in all mutants were confirmed by DNA sequence analyses. CAD and IDUA wild type and mutant mini gene constructs were described by Li et al., Supra. CAD mutant 25 was prepared using the QuickChange PCR-based mutagenesis method (Stratagene). It was derived from CAD1 by a frame-shift mutation that eliminated the 4 intronic in-frame stop codons, and introduced a new in-frame stop codon (S#45). All constructs were confirmed by DNA sequence analysis. A wild type (WT) hUpf1 construct and a construct expressing a dominant negative hUpf1 mutant [Lykke-Andersen (2000) Cell 103:1121-1131] were kindly provided by Dr. Jens Lykke Andersen (Yale University). Suppressor tRNA constructs [Li (1997) J. Exp. Med. 185:985-992] were kindly provided by Dr. Miles Wilkinson (University of Texas, Houston). A WT β-globin construct (pmCMV-Gl-Normal) and a construct expressing a PTC-containing β-globin mRNA [pmCMV-GI-39Ter were provided by Dr. Lynne E. Maquat (University of Rochester) Zhang (1998) RNA 4:801-815].

Cells and transfections—Human 293T cells were grown to 50% confluence in tissue culture plates as described by (44), and transiently co-transfected with the appropriate test DNA construct (2-10 μg per 5×106 293T cells) and pEGFP-N3 (Clontech) (1 μg per 5×106 293T cells) using the calcium phosphate method (Kingston, 1992). Treatment with CHX was as described hereinabove. Treatment with G-418 was effected for 18 hours with the indicated concentrations. The experiments with suppressor tRNAs were performed by co-transfection of the test DNA constructs with pEGFP-N3 and the cognate suppressor tRNA (4 or 12 μg per 5×106 293T cells). In the hUpf1 experiments, cells were co-transfected with the test DNA construct, pEGFP-N3 and the appropriate hUpf1 construct (8 μg per 5×106 293T cells). Cells were harvested 24 or 48 hours following transfection and total cellular RNA was prepared as previously described by (44).

RT-PCR analyses—Splicing products of CAD constructs were analyzed as described in Example 1. RT-PCR reactions of the IDUA RNA spliced products were done as described In Example 1, with the following changes: The primer used for the RT reaction was complementary to the SP6 promoter sequence of the plasmid (SP6 primer, SEQ ID NO: 30), and radioactive PCR was performed using 5′ ³²P-labeled primer c (see Table 2). IDUA PCR products were analyzed by running on 5% polyacrylamide/urea denaturing gels. RT of HTH RNA was performed with the SP6 primer followed by PCR, using primers: HTH primer n [+] 5′-AAGCAGGCAGAGGCCCATCAT-3′, SEQ ID NO: 35; HTH primer k [+] 5′-ATGGTAAGAGGGCAG-3′, SEQ ID NO: 36, and HTH primer f [−] 5′-AGAAGAGCAGGTTTAGCACGG-3′, SEQ ID NO: 37. PCR was performed as previously described [Li (2002) supra], but at an annealing temperature of 58° C., in 3 mM MgCl₂ (primers n+f), or at an annealing temperature of 62° C. (primers k+f). Analysis of PCR products of primers n+f was done by running on a 10% polyacrylamide/urea denaturing gel, followed by Southern hybridization with a ³²P-labeled anti-sense RNA probe. Analysis of PCR products of primers k+f was performed by running on a 2% agarose gel and staining with ethidium bromide.

Results

HTH encodes for a key enzyme in the synthesis of cathecolamines [Grima (1987) Nature 326:707-711], unlike the IDUA and CAD gene systems, HTH has two adjacent alternative 5′SS in the first intron thereof (FIG. 11 a), both of which are used in normal tissues. Because these alternative 5′SS are 12 nucleotides apart, splicing from either site retains the same open reading frame in the expressed product. For this reason the HTH system was selected to examine the effect of in-frame stop codon insertion on suppression of splicing.

Point mutations were Inserted in the wild type HTH mini-gene construct (FIG. 11 a) changing the CAG in codon 4 of exon 1a to TAG (HTH Mut 1) or to GAG (HTH Mut 2). Each of the three constructs was transfected into 293T cells, total RNA was prepared 24 hours following transfection, and subjected to RT-PCR using a primer in the first exon and a primer in exon 3 (primers n and f, respectively). The PCR products were resolved on denaturing gels and detected by Southern blotting.

As shown In FIG. 11 b, the wild type construct (WT) underwent splicing from both 5′ splice sites. Upon insertion of a stop codon between these sites (Mut 1), the product that includes exon la was not detected, while a sense mutation in codon 4 (CAG to GAG, Mut 2) retained the wild type phenotype. To demonstrate that the failure to detect the inclusion of exon la in HTH Mut 1 was not attributable to competition from the PCR product in which exon 1a was excluded, a second PCR was performed using primers that are specific to the exon la included RNA (primers k and f). As shown in FIG. 11 c, even under these conditions, the inclusion of exon 1a was not detected in Mut 1, indicating that splicing from the downstream 5′ splice site in Mut 1 was inactivated, as expected for a latent 5′ splice site subjected to SOS.

Latent splicing is not activated by CHX, an inhibitor of translation known to abrogate NMD—A possible interpretation of our results is that latent splicing normally occurs in pre-mRNAs derived from constructs harboring in-frame stop codons, but the presence of the stop codon sends the spliced transcript, which now harbors a pre-mature translation termination (PTC) codon, to the NMD pathway, where it is rapidly and efficiently degraded. To rule out this possibility, it was previously shown that the protein synthesis inhibitor cycloheximide (CHX), which had already been shown to efficiently reverse the down regulatory effects of PTCs in exons of the T cell receptor-b, the β-globin mRNAs [Carter et al., (1995) J. Biol. Chem. 270:28995-29003], and in the HEXA mRNA [Rajavel and Neufeld (2001) Mol. Cell Biol. 21:5512-5519], did not activate latent splicing in CAD constructs harboring in-frame stop codons between the normal and the latent sites [Li et al., (2002) supra]. Interestingly transcripts derived from HTH and IDUA mini genes behave similarly. Thus, treatment with CHX for up to 270 min of cells transfected with HTH Mut 1, which harbors an in-frame stop codon between the two alternative 5′ splice sites, did not reveal latent splicing that includes exon 1a (FIG. 12 a, lanes 6-10). As a control, the same treatment of cells transfected with wild type HTH, were shown to have virtually no effect on the levels of the exon 1a included-, and exon 1a excluded-splice variants that are normally expressed in wild type HTH (FIG. 12 a, lanes 1-5). Similarly, FIG. 12 b (lanes 1-4) shows that treatment with CHX did not reveal latent splicing in a wild type IDUA construct that harbors an in-frame stop codon downstream of a latent 5′ splice site (FIG. 10). The control shows that when this stop codon was eliminated in IDUA Mut 1 (TGA to TGG mutation), latent splicing was activated but the level of the latent RNA was not affected by the drug (FIG. 12 b, lanes 5-8). A β-globin RNA from cells transfected with pmCMV-GI-39Ter, which harbors a PTC within a bonafide exon [Zhang et al., (1998) RNA 4:801-815] was used as a control. The low level of nonsense β-globin RNA transcribed from this construct increased upon treatment with CHX, indicating that NMD was abrogated [Li et al., (2002) supra and data not shown].

Latent splicing is not activated by G-418, a drug that enables translation read-through—To further show that the null phenotype of latent splicing is not due to NMD, the aminoglycoside antibiotic G-418 was used. This drug is known to abrogate NMD [Bedwell et al. (1997) Nat. Med. 3:1280-1284; Howard et al. (1996) Nat. Med. 2:467-469] by allowing translation read-through of PTC-containing RNAs. Thus, cells transfected with HTH or IDUA mini-genes were treated with different concentrations of G-418 for 18 hr. Here again, latent splicing was not detected in cells transfected with HTH Mut 1 (FIG. 13 a, lanes 6-10), nor in cells transfected with IDUA WT (FIG. 13 b, lanes 1-4) even at a G-418 concentration of 200 mg/ml, as expected for SOS in pre-mRNAs that harbor intronic in-frame stop codons. The negative controls show that the level of exon la inclusion in HTH WT (FIG. 13 a, lanes 1-5) and the level of latent splicing in IDUA Mut 1 (FIG. 13 b, lanes 5-8) were not significantly affected by the G-418 treatment.

Latent splicing is not affected by suppressor tRNA—Suppressor tRNAs enable translation read-through of nonsense mRNAs and were previously shown to be an effective means to abrogate NMD [Li et al. (1997) J. Exp. Med. 185:985-992]. To test whether suppressor tRNAs can reveal latent splicing, each of three different constructs of CAD mutants derived from CAD2 (FIG. 10, CAD), each having a different stop codon (S86) between the normal and the latent 5′ splice sites (CAD Mut 2—TGA; CAD Mut 10—TAG; CAD Mut 11—TAA), were co-transfected with the cognate suppressor tRNA. As can be seen in FIG. 14 a, no latent splicing was observed in RNAs arising from these transfections (lanes 1-9), while in transfection experiments using CAD Mut 12, in which the TGA stop codon at S86 was mutated to TGG (lanes 10-12), the expected latent splicing was observed but, was not affected by co-transfection with suppressor tRNA. Co-transfection experiments with the cognate suppressor tRNAs were also performed with HTH and IDUA constructs (FIGS. 14 b and 14 c, respectively). Here again, the null phenotype of latent splicing was maintained in cells transfected with either HTH Mut 1 (FIG. 14 b, lanes 1-3) or IDUA WT (FIG. 14 c, lanes 1-2) and the respective cognate suppressor tRNA, as expected for SOS in pre-mRNAs that harbor intronic in-frame stop codons upstream of a latent 5′ splice site. As a control β-globin constructs was co-transfected with similar levels of the cognate suppressor tRNA. Transfection with wild type β-globin, with or without suppressor tRNA, gave rise to similar levels of β-globin RNA (FIG. 14 d, lanes 1, 2). Transfection with β-globin 39Ter alone gave rise to a low level of the nonsense β-globin RNA (FIG. 14 d, lane 3), which was up regulated to almost the wild type level by the suppressor tRNA due to abrogation of NMD (FIG. 14 d, lane 4).

Latent splicing is not affected by a dominant negative mutant of hupf1—Human Upf1 is one of a number of proteins directly involved in the NMD pathway [Lykke-Andersen et al., (2000) Cell 103:1121-1131; Lykke-Andersen et al., (2001) Science 293:1836-1839; Mendell et al., (2000) Mol. Cell Biol. 20:8944-8957; Sun et al., (1998) Proc. Natl. Acad. Sci. USA 95:10009-10014]. A dominant negative mutant of hUpf1, in which an arginine at residue 844 was mutated to cysteine (R844C), was shown to abrogate NMD [Lykke-Andersen et al., (2000) supra; Sun et al., (1998) supra]. Therefore is was possible to test directly whether the absence of latent splicing could be attributable to NMD in co-transfection experiments with wild type and mutant hUpf1 constructs. For the CAD system a wild type construct CAD 1, which harbors four in-frame stop codons upstream of the latent 5′ splice site (FIG. 10, CAD) was used along with two mutant constructs: (i) CAD Mut 25 was derived from CAD 1 by a T insertion at position 25, which frame-shifted the four in-frame stop codons and introduced a new one at position 45; and (ii) CAD Mut 9, which has no stop codons upstream of the latent 5′ splice site (Li et al., 1997). FIG. 15 a shows that the null phenotype of latent splicing in CAD Mut 25 and CAD1 (lanes 1 and 4, respectively) was not affected by co-transfection with either wild type hUpf1 (lanes 2 and 5, respectively) or by the dominant negative mutant of hUpf1 (lanes 3 and 6, respectively). Whereas the latent splicing observed in a control of CAD Mut 9 (lane 7) was not significantly affected in the presence of either hUpf1 constructs (lanes 8 and 9). HTH and IDUA were also tested to see if hUpf1 has an effect on them. HTH wild type (no in-frame stop codons) and Mut 1 (one in-frame stop codon) constructs were each co-transfected with either wild type or mutant hUpf1. As expected, neither hUpf1 constructs had any effect on the splicing of HTH wild type (FIG. 15 b lanes 2 and 3). The dominant negative mutant of hUpf1 also had no effect on latent splicing, since it did not activate latent splicing in HTH Mut 1 (FIG. 15 b, lane 6). The co-transfection of either IDUA wild type (one in-frame stop codon) and Mut 1 (no in-frame stop codons), with both hUpf1 constructs had no effect on the splicing pattern of both constructs (FIG. 15 c), further showing that the dominant negative mutant of hUpf1 does not disrupt the SOS mechanism. As a positive control β-globin constructs were co-transfected with similar levels of the hUpf1 constructs. Transfection with β-globin 39Ter alone gave rise to a low level of the nonsense β-globin RNA (FIG. 15 d, lane 4) relative to that of wild type β-globin RNA (FIG. 15 d, lane 1). This level remained unchanged in co-transfection with wild type hUpf1 (FIG. 15 d, lane 5), but was up regulated by the mutant hUpf1 (FIG. 15 d, lane 6).

Table 6—Database of Genes having Putative Latent Splice Sites

Each row includes the following information from left to right <GenBank Accession No.><Number of intron which includes the latent site/s><The coordinate of the latent site/s in the intron (in nt, counted from the 5 end of the intron)><The position of the first stop codon (in nt, counted from the 5′ end of the intron>. TABLE 6 Database of genes having putative latent splice sites Intron Latents First Accession no. No. Pos. Stop codon HSCOMT2 2 168 HSCOMT2 2 228 106 HSCOMT2 3 168 91 HUMCYC1A 1 464 HUMCYC1A 1 528 HUMCYC1A 1 554 313 HUMCYC1A 2 48 74 HUMCYC1A 6 21 no-stop HSU37106 1 13 HSU37106 1 24 HSU37106 1 116 HSU37106 1 162 187 HSU37106 2 105 24 HSGTRH 1 116 HSGTRH 1 296 HSGTRH 1 603 HSGTRH 1 608 HSGTRH 1 935 31 HSGTRH 2 45 HSGTRH 2 1582 HSGTRH 2 1731 HSGTRH 2 2109 7 HUMGALK1A 1 663 HUMGALK1A 1 729 25 HUMGALK1A 2 315 33 HUMGALK1A 5 511 HUMGALK1A 5 766 HUMGALK1A 5 903 HUMGALK1A 5 1199 HUMGALK1A 5 1584 HUMGALK1A 5 2361 HUMGALK1A 5 2450 HUMGALK1A 5 2458 HUMGALK1A 5 2576 HUMGALK1A 5 2669 HUMGALK1A 5 2874 HUMGALK1A 5 2878 HUMGALK1A 5 3538 168 HSU01102 1 148 HSU01102 1 1002 HSU01102 1 1042 HSU01102 1 1274 HSU01102 1 1541 HSU01102 1 1899 HSU01102 1 2077 HSU01102 1 2430 HSU01102 1 2604 192 HSU01102 2 714 163 HSC1INHIB 1 486 HSC1INHIB 1 585 HSC1INHIB 1 589 HSC1INHIB 1 595 HSC1INHIB 1 605 HSC1INHIB 1 1189 HSC1INHIB 1 1202 82 HSC1INHIB 2 26 HSC1INHIB 2 274 HSC1INHIB 2 359 HSC1INHIB 2 615 HSC1INHIB 2 806 HSC1INHIB 2 1077 HSC1INHIB 2 1122 HSC1INHIB 2 1233 HSC1INHIB 2 1389 HSC1INHIB 2 1420 213 HSC1INHIB 3 131 HSC1INHIB 3 156 HSC1INHIB 3 359 HSC1INHIB 3 371 HSC1INHIB 3 667 HSC1INHIB 3 687 HSC1INHIB 3 833 HSC1INHIB 3 851 HSC1INHIB 3 1104 HSC1INHIB 3 1160 HSC1INHIB 3 1455 HSC1INHIB 3 1750 HSC1INHIB 3 1768 HSC1INHIB 3 1840 HSC1INHIB 3 2118 HSC1INHIB 3 2155 HSC1INHIB 3 2159 HSC1INHIB 3 2601 HSC1INHIB 3 2699 HSC1INHIB 3 2969 HSC1INHIB 3 2999 HSC1INHIB 3 3228 HSC1INHIB 3 3337 HSC1INHIB 3 3735 42 HSC1INHIB 5 251 HSC1INHIB 5 339 HSC1INHIB 5 413 HSC1INHIB 5 1416 HSC1INHIB 5 1717 HSC1INHIB 5 1840 HSC1INHIB 5 1845 HSC1INHIB 5 1858 HSC1INHIB 5 2106 HSC1INHIB 5 2440 HSC1INHIB 5 2502 HSC1INHIB 5 2802 HSC1INHIB 5 2816 HSC1INHIB 5 3047 HSC1INHIB 5 3494 HSC1INHIB 5 3747 HSC1INHIB 5 3776 HSC1INHIB 5 3809 HSC1INHIB 5 4570 HSC1INHIB 5 4659 HSC1INHIB 5 4710 10 HSC1INHIB 6 135 HSC1INHIB 6 190 HSC1INHIB 6 323 HSC1INHIB 6 332 HSC1INHIB 6 907 HSC1INHIB 6 1086 HSC1INHIB 6 1267 HSC1INHIB 6 1422 HSC1INHIB 6 1693 69 HSCST4 1 160 HSCST4 1 263 HSCST4 1 601 HSCST4 1 852 HSCST4 1 1128 HSCST4 1 1219 HSCST4 1 1223 HSCST4 1 1687 145 HSCST4 2 12 HSCST4 2 53 HSCST4 2 67 HSCST4 2 183 HSCST4 2 361 HSCST4 2 385 HSCST4 2 411 HSCST4 2 423 HSCST4 2 445 HSCST4 2 1029 HSCST4 2 1104 10 HUMA1ATP 1 549 HUMA1ATP 1 567 HUMA1ATP 1 696 HUMA1ATP 1 1284 HUMA1ATP 1 1332 21 HUMA1ATP 2 210 HUMA1ATP 2 218 HUMA1ATP 2 531 HUMA1ATP 2 569 HUMA1ATP 2 966 HUMA1ATP 2 1149 HUMA1ATP 2 1192 2 HUMA1ATP 3 483 HUMA1ATP 3 760 13 HSINT2 1 1635 HSINT2 1 2040 HSINT2 1 2125 HSINT2 1 2171 384 HSINT2 2 17 HSINT2 2 240 HSINT2 2 309 HSINT2 2 4050 HSINT2 2 4981 HSINT2 2 5118 HSINT2 2 5423 HSINT2 2 5506 31 HUMRBPA 2 4 HUMRBPA 2 451 HUMRBPA 2 698 HUMRBPA 2 982 34 HUMRBPA 3 105 HUMRBPA 3 184 HUMRBPA 3 352 HUMRBPA 3 719 HUMRBPA 3 919 HUMRBPA 3 1074 HUMRBPA 3 1102 HUMRBPA 3 1367 HUMRBPA 3 1388 HUMRBPA 3 1665 HUMRBPA 3 1704 156 HUMRBPA 4 98 HUMRBPA 4 116 HUMRBPA 4 1320 HUMRBPA 4 1598 HUMRBPA 4 1660 HUMRBPA 4 1715 HUMRBPA 4 1798 HUMRBPA 4 1984 HUMRBPA 4 2074 HUMRBPA 4 2553 HUMRBPA 4 2596 HUMRBPA 4 2691 217 HUMRBPA 5 611 HUMRBPA 5 888 124 HUMHSKPQZ7 1 417 2 HUMHSKPQZ7 3 151 90 HUMHSKPQZ7 4 128 HUMHSKPQZ7 4 182 HUMHSKPQZ7 4 210 HUMHSKPQZ7 4 281 HUMHSKPQZ7 4 480 2 HSLH01 1 129 HSLH01 1 223 76 HSBGPG 2 5 HUMGAD45A 1 371 2 HUMGAD45A 3 84 HUMGAD45A 3 88 HUMGAD45A 3 234 HUMGAD45A 3 521 HUMGAD45A 3 525 HUMGAD45A 3 548 HUMGAD45A 3 750 HUMGAD45A 3 781 HUMGAD45A 3 826 HUMGAD45A 3 883 70 HSU50871 1 129 HSU50871 1 263 HSU50871 1 319 HSU50871 1 379 HSU50871 1 1174 217 HSU50871 2 31 HSU50871 2 260 HSU50871 2 304 HSU50871 2 441 HSU50871 2 717 HSU50871 2 762 HSU50871 2 852 HSU50871 2 1074 HSU50871 2 1267 HSU50871 2 1273 HSU50871 2 1300 HSU50871 2 1419 HSU50871 2 1557 2 HSU50871 3 331 HSU50871 3 861 HSU50871 3 936 HSU50871 3 983 HSU50871 3 1240 HSU50871 3 1456 HSU50871 3 1706 HSU50871 3 1731 HSU50871 3 1938 70 HSU50871 4 533 HSU50871 4 570 2 HSU50871 5 3 HSU50871 5 327 HSU50871 5 586 HSU50871 5 590 87 HSU50871 6 714 6 HSU50871 7 118 HSU50871 7 219 126 HSU50871 8 231 HSU50871 8 382 HSU50871 8 405 HSU50871 8 706 HSU50871 8 796 HSU50871 8 818 HSU50871 8 848 HSU50871 8 1538 HSU50871 8 1722 HSU50871 8 1944 HSU50871 8 2048 183 HSU50871 9 173 HSU50871 9 189 HSU50871 9 225 HSU50871 9 317 HSU50871 9 1095 HSU50871 9 1100 HSU50871 9 1114 85 D84344S3 1 49 19 D84344S3 2 26 159 D84344S3 3 43 D84344S3 3 106 56 AF001689 1 396 12 AF001689 2 48 AF001689 2 248 AF001689 2 405 AF001689 2 761 AF001689 2 835 77 AF001689 3 385 83 HSU31929 1 117 HSU31929 1 231 HSU31929 1 753 HSU31929 1 776 HSU31929 1 787 HSU31929 1 1499 HSU31929 1 1729 HSU31929 1 2395 HSU31929 1 2869 HSU31929 1 3020 HSU31929 1 3191 HSU31929 1 3345 120 HSU65896 1 88 132 HSU65896 2 379 HSU65896 2 445 HSU65896 2 487 HSU65896 2 819 HSU65896 2 843 HSU65896 2 916 HSU65896 2 1183 HSU65896 2 1320 273 HSU65896 3 61 HSU65896 3 202 24 HSU65896 4 115 HSU65896 4 130 HSU65896 4 231 HSU65896 4 355 HSU65896 4 468 HSU65896 4 494 HSU65896 4 1035 HSU65896 4 1077 HSU65896 4 1433 HSU65896 4 1515 HSU65896 4 1540 HSU65896 4 1756 59 HSU65896 6 49 HSU65896 6 264 HSU65896 6 695 2 HSU65896 7 261 HSU65896 7 292 HSU65896 7 310 12 HSU65896 8 111 40 HSU65896 9 144 HSU65896 9 202 HSU65896 9 342 82 HSU65896 10 184 HSU65896 10 232 HSU65896 10 385 HSU65896 10 389 32 HSU65896 11 11 HSU65896 11 123 HSU65896 11 149 96 HSU65896 12 81 HSU65896 12 283 16 HSU65896 14 48 HSU65896 14 113 HSU65896 14 348 2 HSSHBG 6 466 HSSHBG 6 553 HSSHBG 6 604 HSSHBG 6 661 106 HUMDEF5A 1 350 HUMDEF5A 1 467 HUMDEF5A 1 624 HUMDEF5A 1 708 HUMDEF5A 1 727 HUMDEF5A 1 751 93 HSU60477 1 48 HSU60477 1 72 HSU60477 1 243 HSU60477 1 1442 75 HSU60477 2 782 HSU60477 2 833 HSU60477 2 905 HSU60477 2 1284 HSU60477 2 1794 HSU60477 2 1899 39 AF034632 1 294 AF034632 1 509 AF034632 1 661 219 HUMHPRTB 1 196 HUMHPRTB 1 397 HUMHPRTB 1 607 HUMHPRTB 1 1098 HUMHPRTB 1 1272 HUMHPRTB 1 1732 HUMHPRTB 1 1794 HUMHPRTB 1 2078 HUMHPRTB 1 2556 HUMHPRTB 1 2645 HUMHPRTB 1 2665 HUMHPRTB 1 2703 HUMHPRTB 1 2767 HUMHPRTB 1 2810 HUMHPRTB 1 3292 HUMHPRTB 1 3745 HUMHPRTB 1 4063 HUMHPRTB 1 4104 HUMHPRTB 1 4506 HUMHPRTB 1 4842 HUMHPRTB 1 5107 HUMHPRTB 1 5246 HUMHPRTB 1 5319 HUMHPRTB 1 5395 HUMHPRTB 1 5399 HUMHPRTB 1 5722 HUMHPRTB 1 5850 HUMHPRTB 1 5866 HUMHPRTB 1 5978 HUMHPRTB 1 6133 HUMHPRTB 1 6198 HUMHPRTB 1 6296 HUMHPRTB 1 6365 HUMHPRTB 1 6542 HUMHPRTB 1 6591 HUMHPRTB 1 6839 HUMHPRTB 1 6948 HUMHPRTB 1 7091 HUMHPRTB 1 7226 HUMHPRTB 1 7402 HUMHPRTB 1 7845 HUMHPRTB 1 7906 HUMHPRTB 1 8145 HUMHPRTB 1 8204 HUMHPRTB 1 8884 HUMHPRTB 1 9070 HUMHPRTB 1 9074 HUMHPRTB 1 9359 HUMHPRTB 1 9381 HUMHPRTB 1 9543 HUMHPRTB 1 9636 HUMHPRTB 1 10277 HUMHPRTB 1 10289 HUMHPRTB 1 10311 HUMHPRTB 1 10371 HUMHPRTB 1 10987 HUMHPRTB 1 11221 HUMHPRTB 1 11323 HUMHPRTB 1 11403 HUMHPRTB 1 11535 HUMHPRTB 1 11731 HUMHPRTB 1 11774 HUMHPRTB 1 12470 HUMHPRTB 1 12705 HUMHPRTB 1 12995 400 HUMHPRTB 2 3 HUMHPRTB 2 320 HUMHPRTB 2 1097 HUMHPRTB 2 1277 HUMHPRTB 2 1517 HUMHPRTB 2 1558 HUMHPRTB 2 1625 HUMHPRTB 2 1653 2 HUMHPRTB 3 201 HUMHPRTB 3 356 HUMHPRTB 3 474 HUMHPRTB 3 676 HUMHPRTB 3 923 HUMHPRTB 3 1098 HUMHPRTB 3 1572 HUMHPRTB 3 1839 HUMHPRTB 3 1932 HUMHPRTB 3 2409 HUMHPRTB 3 2452 HUMHPRTB 3 2655 HUMHPRTB 3 2753 HUMHPRTB 3 2796 HUMHPRTB 3 2992 HUMHPRTB 3 3019 HUMHPRTB 3 3553 HUMHPRTB 3 3606 HUMHPRTB 3 3830 HUMHPRTB 3 3838 HUMHPRTB 3 4384 HUMHPRTB 3 4455 HUMHPRTB 3 4633 HUMHPRTB 3 4820 HUMHPRTB 3 4840 HUMHPRTB 3 5222 HUMHPRTB 3 5671 HUMHPRTB 3 5940 HUMHPRTB 3 6029 HUMHPRTB 3 6244 HUMHPRTB 3 6376 HUMHPRTB 3 6435 HUMHPRTB 3 6669 HUMHPRTB 3 7210 HUMHPRTB 3 7594 HUMHPRTB 3 8076 HUMHPRTB 3 8367 HUMHPRTB 3 8372 HUMHPRTB 3 8529 HUMHPRTB 3 8534 HUMHPRTB 3 8864 HUMHPRTB 3 8913 HUMHPRTB 3 9009 HUMHPRTB 3 9233 HUMHPRTB 3 9354 HUMHPRTB 3 10148 HUMHPRTB 3 11059 19 HUMHPRTB 4 135 HUMHPRTB 4 312 HUMHPRTB 4 322 HUMHPRTB 4 385 HUMHPRTB 4 480 HUMHPRTB 4 489 HUMHPRTB 4 567 HUMHPRTB 4 787 HUMHPRTB 4 1037 HUMHPRTB 4 1348 HUMHPRTB 4 1564 HUMHPRTB 4 1708 HUMHPRTB 4 2106 HUMHPRTB 4 2384 HUMHPRTB 4 2639 HUMHPRTB 4 2788 HUMHPRTB 4 3051 HUMHPRTB 4 3120 HUMHPRTB 4 3133 HUMHPRTB 4 3244 HUMHPRTB 4 3258 HUMHPRTB 4 3431 HUMHPRTB 4 3589 85 HUMHPRTB 5 66 HUMHPRTB 5 1299 HUMHPRTB 5 1668 HUMHPRTB 5 1714 HUMHPRTB 5 1718 HUMHPRTB 5 1730 HUMHPRTB 5 3188 25 HUMHPRTB 6 51 HUMHPRTB 6 308 HUMHPRTB 6 565 HUMHPRTB 6 789 HUMHPRTB 6 818 HUMHPRTB 6 898 HUMHPRTB 6 962 HUMHPRTB 6 1261 HUMHPRTB 6 1373 HUMHPRTB 6 1429 HUMHPRTB 6 1517 HUMHPRTB 6 1699 HUMHPRTB 6 1914 HUMHPRTB 6 2579 HUMHPRTB 6 2965 HUMHPRTB 6 3104 HUMHPRTB 6 3200 HUMHPRTB 6 3228 HUMHPRTB 6 3256 HUMHPRTB 6 3335 HUMHPRTB 6 3980 HUMHPRTB 6 4120 HUMHPRTB 6 4136 HUMHPRTB 6 4382 HUMHPRTB 6 4568 HUMHPRTB 6 4665 HUMHPRTB 6 4725 8 HUMHPRTB 7 3 6 HUMHPRTB 8 3 HUMHPRTB 8 265 HUMHPRTB 8 580 HUMHPRTB 8 660 HUMHPRTB 8 904 HUMHPRTB 8 1317 94 HSCKBG 3 299 246 HSCKBG 4 189 HSCKBG 4 257 HSCKBG 4 262 197 HSCKBG 5 45 AF010238 1 500 AF010238 1 839 AF010238 1 900 AF010238 1 1682 AF010238 1 1700 AF010238 1 2633 AF010238 1 2723 AF010238 1 2766 AF010238 1 2783 AF010238 1 2798 AF010238 1 3031 AF010238 1 3105 AF010238 1 3109 AF010238 1 3664 AF010238 1 3930 AF010238 1 3947 AF010238 1 4274 105 AF010238 2 39 AF010238 2 250 AF010238 2 719 AF010238 2 829 AF010238 2 871 AF010238 2 964 AF010238 2 1274 AF010238 2 1363 AF010238 2 1436 AF010238 2 1525 AF010238 2 1589 AF010238 2 1628 AF010238 2 2146 AF010238 2 2179 AF010238 2 2944 AF010238 2 3047 AF010238 2 3069 42 HUMBHSD 1 20 HUMBHSD 1 48 HUMBHSD 1 479 HUMBHSD 1 497 HUMBHSD 1 501 HUMBHSD 1 651 HUMBHSD 1 1564 HUMBHSD 1 2455 HUMBHSD 1 2548 HUMBHSD 1 2644 HUMBHSD 1 2802 HUMBHSD 1 2862 HUMBHSD 1 3178 6 HUMBHSD 2 30 HUMBHSD 2 199 HUMBHSD 2 222 HUMBHSD 2 226 HUMBHSD 2 234 HUMBHSD 2 523 HUMBHSD 2 1138 HUMBHSD 2 1486 HUMBHSD 2 1704 HUMBHSD 2 1717 HUMBHSD 2 1968 87 HSREP10 1 406 HSREP10 1 750 409 HSREP10 2 23 HSREP10 3 162 HSREP10 3 344 HSREP10 3 405 HSREP10 3 706 HSREP10 3 909 HSREP10 3 941 HSREP10 3 1031 HSREP10 3 1400 HSREP10 3 1549 HSREP10 3 1627 HSREP10 3 1657 HSREP10 3 1945 HSREP10 3 2387 HSREP10 3 2580 HSREP10 3 2584 HSREP10 3 2681 HSREP10 3 3547 HSREP10 3 3921 HSREP10 3 3963 HSREP10 3 4211 HSREP10 3 4611 HSREP10 3 4676 HSREP10 3 4798 51 HUMIL5 1 40 43 HUMIL5 2 40 HUMIL5 2 279 HUMIL5 2 450 HUMIL5 2 743 HUMIL5 2 858 7 HUMBFXIII 1 390 HUMBFXIII 1 512 HUMBFXIII 1 595 HUMBFXIII 1 713 HUMBFXIII 1 1163 HUMBFXIII 1 1588 HUMBFXIII 1 1711 HUMBFXIII 1 1715 HUMBFXIII 1 1780 HUMBFXIII 1 2076 HUMBFXIII 1 2566 HUMBFXIII 1 2646 HUMBFXIII 1 3340 HUMBFXIII 1 3471 HUMBFXIII 1 3501 HUMBFXIII 1 3974 15 HUMBFXIII 2 274 HUMBFXIII 2 495 HUMBFXIII 2 574 72 HUMBFXIII 3 155 HUMBFXIII 3 391 HUMBFXIII 3 538 HUMBFXIII 3 662 18 HUMBFXIII 4 282 150 HUMBFXIII 5 532 HUMBFXIII 5 819 HUMBFXIII 5 889 HUMBFXIII 5 1234 HUMBFXIII 5 1371 HUMBFXIII 5 1672 HUMBFXIII 5 1841 HUMBFXIII 5 2044 HUMBFXIII 5 2083 HUMBFXIII 5 2205 HUMBFXIII 5 2245 HUMBFXIII 5 2764 60 HUMBFXIII 6 56 3 HUMBFXIII 7 155 HUMBFXIII 7 279 HUMBFXIII 7 328 HUMBFXIII 7 434 HUMBFXIII 7 675 HUMBFXIII 7 918 30 HUMBFXIII 8 42 HUMBFXIII 8 593 HUMBFXIII 8 704 HUMBFXIII 8 774 HUMBFXIII 8 911 HUMBFXIII 8 1266 HUMBFXIII 8 1629 HUMBFXIII 8 2124 HUMBFXIII 8 2488 HUMBFXIII 8 2508 45 HUMBFXIII 9 169 HUMBFXIII 9 1477 HUMBFXIII 9 1626 36 HUMBFXIII 10 225 HUMBFXIII 10 262 HUMBFXIII 10 1149 HUMBFXIII 10 1843 HUMBFXIII 10 1903 HUMBFXIII 10 2393 HUMBFXIII 10 2450 HUMBFXIII 10 2519 HUMBFXIII 10 2594 HUMBFXIII 10 2661 HUMBFXIII 10 2856 HUMBFXIII 10 2897 HUMBFXIII 10 3800 HUMBFXIII 10 3826 HUMBFXIII 10 4198 HUMBFXIII 10 4233 HUMBFXIII 10 4250 HUMBFXIII 10 4269 HUMBFXIII 10 4560 HUMBFXIII 10 4640 HUMBFXIII 10 4675 HUMBFXIII 10 5706 HUMBFXIII 10 5830 HUMBFXIII 10 6747 HUMBFXIII 10 6949 HUMBFXIII 10 6987 HUMBFXIII 10 7804 HUMBFXIII 10 7993 HUMBFXIII 10 8129 HUMBFXIII 10 8131 HUMBFXIII 10 8527 HUMBFXIII 10 9085 HUMBFXIII 10 9089 HUMBFXIII 10 9112 HUMBFXIII 10 9439 HUMBFXIII 10 9483 12 HUMBFXIII 11 711 HUMBFXIII 11 885 HUMBFXIII 11 975 2 HUMSAP01 1 7 HUMSAP01 1 33 HUMSAP01 1 85 36 HUMCRYABA 1 103 HUMCRYABA 1 618 HUMCRYABA 1 690 118 HUMCRYABA 2 423 HUMCRYABA 2 1300 49 HUMROD1X 1 241 2 HUMPRF1A 1 146 HUMPRF1A 1 226 HUMPRF1A 1 275 HUMPRF1A 1 999 2 HS2OXOC 1 356 2 HS2OXOC 5 24 2 HS2OXOC 6 52 HS2OXOC 6 68 88 HUMAPOA4A 2 279 HUMAPOA4A 2 339 HUMAPOA4A 2 531 HUMAPOA4A 2 539 2 HSODF2 1 121 2 HSN10C3 1 252 HSN10C3 1 694 HSN10C3 1 945 HSN10C3 1 974 HSN10C3 1 1873 HSN10C3 1 2078 HSN10C3 1 2420 HSN10C3 1 2525 HSN10C3 1 2889 HSN10C3 1 3024 HSN10C3 1 3047 HSN10C3 1 3722 HSN10C3 1 3808 HSN10C3 1 4320 HSN10C3 1 4555 HSN10C3 1 4992 HSN10C3 1 5235 HSN10C3 1 5432 HSN10C3 1 6369 HSN10C3 1 6634 HSN10C3 1 7031 HSN10C3 1 7386 HSN10C3 1 7682 463 HSN10C3 2 304 HSN10C3 2 766 HSN10C3 2 1562 HSN10C3 2 1655 HSN10C3 2 2212 363 HSN10C3 3 259 HSN10C3 3 540 36 HSN10C3 4 38 HSN10C3 4 100 HSN10C3 4 209 HSN10C3 4 264 HSN10C3 4 523 73 HSN10C3 5 782 HSN10C3 5 925 HSN10C3 5 1140 HSN10C3 5 1792 HSN10C3 5 1819 HSN10C3 5 1987 HSN10C3 5 2249 HSN10C3 5 2256 HSN10C3 5 2444 HSN10C3 5 2582 HSN10C3 5 2744 HSN10C3 5 2758 HSN10C3 5 2879 HSN10C3 5 2893 HSN10C3 5 3153 HSN10C3 5 3205 HSN10C3 5 3274 HSN10C3 5 3278 HSN10C3 5 3433 HSN10C3 5 3747 HSN10C3 5 3872 HSN10C3 5 3991 HSN10C3 5 4078 HSN10C3 5 4171 69 HSU46692 1 361 HSU46692 1 684 43 HSU46692 2 203 HSU46692 2 282 82 HSPROPG 1 7 HSPROPG 2 398 HSPROPG 2 937 HSPROPG 2 1022 HSPROPG 2 1048 HSPROPG 2 1117 HSPROPG 2 1226 113 HSPROPG 3 129 HSPROPG 3 134 HSPROPG 3 143 HSPROPG 3 267 HSPROPG 3 273 HSPROPG 3 323 102 HSPROPG 8 99 HSPROPG 8 546 HSPROPG 8 604 HSPROPG 8 919 HSPROPG 8 1092 HSPROPG 8 1219 2 HSHCC1GEN 1 193 HSHCC1GEN 1 616 HSHCC1GEN 1 818 HSHCC1GEN 1 822 HSHCC1GEN 1 880 HSHCC1GEN 1 1523 HSHCC1GEN 1 1528 HSHCC1GEN 1 1897 135 HSHCC1GEN 2 105 HSHCC1GEN 2 354 HSHCC1GEN 2 359 2 HUMNKG5PRO 1 376 HUMNKG5PRO 1 452 HUMNKG5PRO 1 525 HUMNKG5PRO 1 652 63 HUMNKG5PRO 2 67 HUMNKG5PRO 2 98 HUMNKG5PRO 2 171 HUMNKG5PRO 2 364 70 HUMNKG5PRO 3 133 HUMNKG5PRO 3 199 HUMNKG5PRO 3 624 HUMNKG5PRO 3 1119 58 HUMNKG5PRO 4 11 HUMNKG5PRO 4 182 HUMNKG5PRO 4 603 HUMNKG5PRO 4 768 HUMNKG5PRO 4 787 33 HSG17G 1 434 2 HSG17G 2 90 84 HSG17G 3 18 HSG17G 4 103 65 HSG17G 5 62 88 HSG17G 6 100 24 HUMIGERA 1 82 HUMIGERA 1 258 6 HUMIGERA 2 375 HUMIGERA 2 776 93 HUMIGERA 3 35 HUMIGERA 3 71 HUMIGERA 3 191 HUMIGERA 3 203 HUMIGERA 3 577 HUMIGERA 3 964 HUMIGERA 3 1147 HUMIGERA 3 1337 HUMIGERA 3 1421 HUMIGERA 3 1686 54 HUMIGERA 4 453 HUMIGERA 4 950 HUMIGERA 4 1112 HUMIGERA 4 1193 81 HUMGAPDHG 1 129 HUMGAPDHG 1 282 HUMGAPDHG 1 486 HUMGAPDHG 1 607 HUMGAPDHG 1 620 HUMGAPDHG 1 661 HUMGAPDHG 1 1330 HUMGAPDHG 1 1526 2 HUMGAPDHG 2 13 16 HUMGAPDHG 6 130 4 HSGLUCG2 1 951 HSGLUCG2 1 1340 HSGLUCG2 1 1517 5 HSGLUCG2 2 406 HSGLUCG2 2 951 HSGLUCG2 2 1022 HSGLUCG2 2 1082 HSGLUCG2 2 1387 HSGLUCG2 2 1617 2 HSGLUCG2 3 109 HSGLUCG2 3 542 HSGLUCG2 3 1226 2 HSGLUCG2 4 332 2 HSU20499 1 3 6 HSU20499 2 20 75 HSU20499 3 499 HSU20499 3 835 HSU20499 3 927 HSU20499 3 1056 HSU20499 3 1093 HSU20499 3 1107 133 HSU20499 5 441 31 HSHSC70 1 67 HSHSC70 1 203 HSHSC70 1 242 63 HSHSC70 2 4 HSHSC70 2 149 HSHSC70 2 278 139 HSHSC70 4 44 57 HSHSC70 6 58 HSHSC70 6 106 75 HSRSGCG 2 384 HSRSGCG 2 836 HSRSGCG 2 892 HSRSGCG 2 946 HSRSGCG 2 1796 HSRSGCG 2 1812 HSRSGCG 2 1819 HSRSGCG 2 1823 HSRSGCG 2 1880 HSRSGCG 2 1960 127 HSRSGCG 4 16 HSRSGCG 4 27 HSRSGCG 4 111 HSRSGCG 4 260 2 HSRSGCG 5 203 43 HSRSGCG 6 227 HSRSGCG 6 307 HSRSGCG 6 466 HSRSGCG 6 809 HSRSGCG 6 953 HSRSGCG 6 1237 148 HSRSGCG 7 79 HSRSGCG 7 156 HSRSGCG 7 289 HSRSGCG 7 589 HSRSGCG 7 634 HSRSGCG 7 775 82 HSRSGCG 9 443 168 HSRSGCG 10 384 78 HSRSGCG 11 257 133 HSRSGCG 12 67 92 HSRSGCG 13 190 28 HSRSGCG 15 27 HSRSGCG 15 47 HSMB1GENE 1 207 HSMB1GENE 1 225 HSMB1GENE 1 422 HSMB1GENE 1 949 34 HSMB1GENE 2 372 HSMB1GENE 2 537 HSMB1GENE 2 569 HSMB1GENE 2 693 HSMB1GENE 2 879 HSMB1GENE 2 1007 HSMB1GENE 2 1141 HSMB1GENE 2 1362 HSMB1GENE 2 1497 HSMB1GENE 2 1994 HSMB1GENE 2 2049 HSMB1GENE 2 2140 HSMB1GENE 2 2261 HSMB1GENE 2 2341 HSMB1GENE 2 3107 HSMB1GENE 2 3165 HSMB1GENE 2 3320 45 HUMHSP27X 1 650 195 HUMHSP27X 2 22 HUMHSP27X 2 26 HUMHSP27X 2 76 2 AF042001 1 642 36 AF042001 2 280 AF042001 2 419 AF042001 2 661 AF042001 2 748 AF042001 2 818 87 HUMSTATH2 1 557 HUMSTATH2 1 681 HUMSTATH2 1 760 HUMSTATH2 1 786 HUMSTATH2 1 843 94 HUMSTATH2 3 144 HUMSTATH2 3 349 HUMSTATH2 3 455 HUMSTATH2 3 727 HUMSTATH2 3 854 HUMSTATH2 3 951 13 HSFGFR4G 1 13 HSFGFR4G 1 246 HSFGFR4G 1 263 HSFGFR4G 1 299 HSFGFR4G 1 425 HSFGFR4G 1 625 225 HSFGFR4G 4 178 94 HSFGFR4G 5 112 HSFGFR4G 5 120 HSFGFR4G 5 143 HSFGFR4G 5 382 147 HSFGFR4G 7 75 HSFGFR4G 7 198 282 HSFGFR4G 10 161 HSFGFR4G 10 324 HSFGFR4G 10 393 HSFGFR4G 10 470 HSFGFR4G 10 1018 48 HSFGFR4G 12 234 HSFGFR4G 12 274 4 HSFGFR4G 14 160 2 HSFGFR4G 15 70 2 HUMCD79B 1 391 171 HUMCD79B 2 317 HUMCD79B 2 344 HUMCD79B 2 711 6 HUMCD79B 3 10 30 HUMCD79B 5 39 HUMHOX4A 1 353 HUMHOX4A 1 480 HUMHOX4A 1 484 HUMHOX4A 1 680 HUMHOX4A 1 902 HUMHOX4A 1 1566 HUMHOX4A 1 1649 HUMHOX4A 1 1662 HUMHOX4A 1 1682 HUMHOX4A 1 1686 HUMHOX4A 1 1690 HUMHOX4A 1 1753 135 HSCPH70 1 54 HSCPH70 1 822 HSCPH70 1 994 HSCPH70 1 1206 HSCPH70 1 1321 HSCPH70 1 1470 HSCPH70 1 1945 HSCPH70 1 1967 HSCPH70 1 2032 HSCPH70 1 2101 HSCPH70 1 2165 HSCPH70 1 2169 HSCPH70 1 2324 64 HSCPH70 2 78 15 HSCPH70 4 449 HSCPH70 4 1263 2 HSALADG 1 103 HSALADG 1 395 HSALADG 1 965 2 HSALADG 3 72 HSALADG 3 169 HSALADG 3 208 HSALADG 3 405 22 HSALADG 6 137 HSALADG 6 151 109 HSALADG 9 9 HSALADG 10 280 HSALADG 10 553 45 HUMIDS 2 25 HUMIDS 2 209 HUMIDS 2 337 HUMIDS 2 510 340 HUMIDS 3 360 HUMIDS 3 438 HUMIDS 3 848 HUMIDS 3 1236 HUMIDS 3 1291 HUMIDS 3 1801 HUMIDS 3 1895 HUMIDS 3 1982 120 HUMIDS 4 140 HUMIDS 4 201 HUMIDS 4 605 HUMIDS 4 619 HUMIDS 4 826 HUMIDS 4 933 HUMIDS 4 1848 HUMIDS 4 2123 10 HUMIDS 5 79 HUMIDS 5 179 HUMIDS 5 277 HUMIDS 5 407 HUMIDS 5 634 HUMIDS 5 1074 HUMIDS 5 1087 HUMIDS 5 1195 HUMIDS 5 1304 HUMIDS 5 1439 37 HUMIDS 6 53 HUMIDS 6 117 HUMIDS 6 159 HUMIDS 6 246 HUMIDS 6 272 HUMIDS 6 322 HUMIDS 6 886 HUMIDS 6 1029 HUMIDS 6 1288 HUMIDS 6 1310 HUMIDS 6 1334 HUMIDS 6 1549 HUMIDS 6 1553 HUMIDS 6 2080 HUMIDS 6 2454 HUMIDS 6 2477 HUMIDS 6 3239 HUMIDS 6 3964 HUMIDS 6 4121 HUMIDS 6 4570 HUMIDS 6 4660 HUMIDS 6 4797 HUMIDS 6 4807 HUMIDS 6 4854 HUMIDS 6 5328 HUMIDS 6 5362 HUMIDS 6 5629 13 HUMIDS 7 21 HUMIDS 7 88 HUMIDS 7 198 HUMIDS 7 204 HUMIDS 7 818 HUMIDS 7 964 HUMIDS 7 978 HUMIDS 7 1361 HUMIDS 7 2250 HUMIDS 7 2455 HUMIDS 7 2672 HUMIDS 7 2809 HUMIDS 7 2931 HUMIDS 7 3067 HUMIDS 7 3077 HUMIDS 7 3096 24 HUMIDS 8 268 HUMIDS 8 478 HUMIDS 8 775 HUMIDS 8 1230 HUMIDS 8 1981 HUMIDS 8 2042 HUMIDS 8 2355 HUMIDS 8 2371 HUMIDS 8 2661 HUMIDS 8 2760 HUMIDS 8 2995 HUMIDS 8 3040 HUMIDS 8 3100 HUMIDS 8 3255 HUMIDS 8 3267 HUMIDS 8 3540 78 HSU82083 1 1173 HSU82083 1 1783 HSU82083 1 2190 106 HSU82083 2 251 HSU82083 2 255 HSU82083 2 263 282 HSU82083 3 566 200 HSU82083 4 296 HSU82083 4 676 HSU82083 4 696 HSU82083 4 884 HSU82083 4 910 HSU82083 4 1101 HSU82083 4 1146 129 HSU82083 5 18 HSU82083 5 45 21 HSU82083 6 94 HSU82083 6 444 HSU82083 6 930 HSU82083 6 944 HSU82083 6 1016 HSU82083 6 1550 30 HSU82083 8 118 HSU82083 8 216 HSU82083 8 703 HSU82083 8 822 HSU82083 8 1655 HSU82083 8 2271 HSU82083 8 2327 HSU82083 8 2338 HSU82083 8 2477 10 HSU82083 9 403 HSU82083 9 445 HSU82083 9 806 HSU82083 9 973 322 HUM17BHSDI 1 9 12 HUM17BHSDI 4 208 HUM17BHSDI 4 213 2 HUMTDGF1A 1 275 HUMTDGF1A 1 407 HUMTDGF1A 1 495 HUMTDGF1A 1 845 HUMTDGF1A 1 853 HUMTDGF1A 1 906 20 HUMTDGF1A 3 133 165 HUMTDGF1A 5 713 HUMTDGF1A 5 816 HUMTDGF1A 5 838 HUMTDGF1A 5 955 HUMTDGF1A 5 957 99 HSALDCG 1 21 HSALDCG 1 32 24 HSALDCG 4 19 22 HSALDCG 7 19 Intron Latents First Accession No. No. Pos. Stop codon HSCTAS 1 62 HSCTAS 1 101 HSCTAS 1 785 HSCTAS 1 1129 HSCTAS 1 1342 HSCTAS 1 1626 HSCTAS 1 1748 6 HSCTAS 2 42 2 HSCTAS 3 3 HSCTAS 3 91 HSCTAS 3 379 HSCTAS 3 490 HSCTAS 3 517 HSCTAS 3 529 HSCTAS 3 666 HSCTAS 3 801 HSCTAS 3 864 94 HSCTAS 4 12 HSCTAS 4 20 HSCTAS 4 387 HSCTAS 4 811 HSCTAS 4 1503 HSCTAS 4 2122 2 HSCTAS 6 92 HSCTAS 6 632 HSCTAS 6 639 HSCTAS 6 781 HSCTAS 6 788 HSCTAS 6 1806 HSCTAS 6 1810 31 HSCTAS 7 242 HSCTAS 7 342 156 HSU27266 1 9 6 HSU27266 2 85 HSU27266 2 185 HSU27266 2 189 HSU27266 2 193 HSU27266 2 249 HSU27266 2 275 HSU27266 2 563 201 HSU27266 3 564 HSU27266 3 632 HSU27266 3 684 HSU27266 3 1089 177 HSU27266 4 149 HSU27266 4 175 HSU27266 4 318 313 HSU27266 6 353 HSU27266 6 551 HSU27266 6 564 HSU27266 6 576 124 HSU27266 7 263 HSU27266 7 306 186 HSU27266 8 42 145 HSU27266 9 96 30 HSU89387 1 261 HSU89387 1 390 HSU89387 1 419 HSU89387 1 1073 HSU89387 1 1208 HSU89387 1 1252 HSU89387 1 1482 HSU89387 1 1695 HSU89387 1 1983 HSU89387 1 2026 HSU89387 1 2412 HSU89387 1 2594 HSU89387 1 2768 HSU89387 1 2869 HSU89387 1 3186 HSU89387 1 3763 HSU89387 1 4124 HSU89387 1 4166 HSU89387 1 4199 HSU89387 1 4203 HSU89387 1 4219 HSU89387 1 4223 HSU89387 1 4663 90 HSU89387 2 386 HSU89387 2 522 HSU89387 2 534 HSU89387 2 580 HSU89387 2 674 HSU89387 2 718 HSU89387 2 1144 HSU89387 2 1212 HSU89387 2 2056 HSU89387 2 2097 2 HSU89387 3 58 HSU89387 3 535 HSU89387 3 641 HSU89387 3 1088 HSU89387 3 1304 HSU89387 3 1316 HSU89387 3 1457 HSU89387 3 1545 HSU89387 3 1700 HSU89387 3 1770 HSU89387 3 1842 HSU89387 3 2105 HSU89387 3 2214 HSU89387 3 2303 38 HSAPOA2 1 191 HSAPOA2 1 207 51 HSFBRGG 4 72 HSFBRGG 4 415 HSFBRGG 4 539 HSFBRGG 4 793 HSFBRGG 4 935 HSFBRGG 4 939 HSFBRGG 4 1072 HSFBRGG 4 1151 2 HSFBRGG 5 38 HSFBRGG 5 59 HSFBRGG 5 184 6 HSFBRGG 6 124 HSFBRGG 6 357 HSFBRGG 6 696 HSFBRGG 6 843 82 HSFBRGG 7 164 HSFBRGG 7 1126 HSFBRGG 7 1231 35 HSFBRGG 8 397 HSFBRGG 8 435 HSFBRGG 8 1426 HSFBRGG 8 1539 HSFBRGG 8 1589 36 HSFBRGG 9 433 61 HSPACAP 1 1863 2 HSPACAP 2 234 2 HSPACAP 3 37 HSPACAP 3 73 HSPACAP 3 95 HSPACAP 3 725 HSPACAP 3 801 2 HUMDS 1 30 HUMDS 1 431 289 HUMDS 2 54 HUMDS 2 365 HUMDS 2 453 HUMDS 2 802 HUMDS 2 1249 HUMDS 2 1424 HUMDS 2 1727 HUMDS 2 1755 HUMDS 2 2106 HUMDS 2 2143 HUMDS 2 2174 HUMDS 2 2477 HUMDS 2 2672 HUMDS 2 2872 57 HUMDS 3 111 HUMDS 3 224 HUMDS 3 306 HUMDS 3 491 HUMDS 3 1093 HUMDS 3 1342 HUMDS 3 1638 HUMDS 3 1778 HUMDS 3 2371 HUMDS 3 2431 HUMDS 3 2463 HUMDS 3 2531 HUMDS 3 2828 HUMDS 3 2909 HUMDS 3 2971 HUMDS 3 3126 HUMDS 3 3156 HUMDS 3 3233 HUMDS 3 3376 HUMDS 3 3407 HUMDS 3 3438 2 HUMDS 5 119 HUMDS 5 257 9 HUMDS 6 405 HUMDS 6 541 HUMDS 6 558 HUMDS 6 645 HUMDS 6 856 49 HUMDS 7 1016 HUMDS 7 1339 HUMDS 7 1383 57 HUMDS 9 245 HUMDS 9 320 HUMDS 9 682 10 HUMDS 10 108 HUMDS 10 674 HUMDS 10 761 HUMDS 10 901 HUMDS 10 1108 HUMDS 10 1201 HUMDS 10 1257 HUMDS 10 1802 HUMDS 10 2126 HUMDS 10 2779 HUMDS 10 3843 HUMDS 10 3933 2 HUMDS 11 38 HUMDS 11 42 HUMDS 11 558 HUMDS 11 1257 171 HUMDS 12 16 88 HUMDS 13 173 HUMDS 13 494 HUMDS 13 640 7 HUMDS 14 354 HUMDS 14 802 43 HSU48795 2 24 46 HSU48795 3 542 130 HSU19816 1 3 HSU19816 1 45 HSU19816 1 425 6 HSODCG 1 130 HSODCG 1 233 HSODCG 1 240 HSODCG 1 252 10 HSODCG 6 404 HSODCG 6 1002 7 HSODCG 9 3 HSODCG 9 161 HSODCG 9 221 HSODCG 9 266 HSODCG 9 437 HSODCG 9 475 HSODCG 9 573 HSODCG 9 599 2 HSU29895 2 270 HSU29895 2 387 34 HSU29895 4 128 109 HSU29895 5 121 HSU29895 6 1020 HSU29895 6 1112 121 HSU29895 7 529 HSU29895 7 571 HSU29895 7 848 HSU29895 7 1416 HSU29895 7 1599 HSU29895 7 1841 HSU29895 7 1955 HSU29895 7 2084 HSU29895 7 2476 HSU29895 7 2561 HSU29895 7 2761 HSU29895 7 3087 HSU29895 7 3105 HSU29895 7 3182 HSU29895 7 3410 HSU29895 7 3492 HSU29895 7 3658 HSU29895 7 3708 HSU29895 7 4282 HSU29895 7 4286 HSU29895 7 4422 46 HSU29895 8 21 HSU29895 8 84 HSU29895 8 352 2 HSU29895 9 143 HSU29895 9 161 HSU29895 9 310 HSU29895 9 455 HSU29895 9 645 HSU29895 9 1089 HSU29895 9 1230 HSU29895 9 1480 HSU29895 9 1525 2 HSU29895 10 69 58 HSU29895 11 413 HSU29895 11 920 HSU29895 11 1123 HSU29895 11 1524 HSU29895 11 1587 HSU29895 11 1744 HSU29895 11 1902 HSU29895 11 2567 HSU29895 11 2571 HSU29895 11 2585 HSU29895 11 2829 247 HSU29895 12 268 HSU29895 12 364 HSU29895 12 445 HSU29895 12 454 HSU29895 12 730 HSU29895 12 985 HSU29895 12 1034 HSU29895 12 1048 HSU29895 12 1194 HSU29895 12 1222 HSU29895 12 1328 HSU29895 12 1470 HSU29895 12 1776 HSU29895 12 1792 HSU29895 12 2092 HSU29895 12 2309 HSU29895 12 2726 HSU29895 12 2863 HSU29895 12 2890 HSU29895 12 3169 HSU29895 12 3529 HSU29895 12 3553 157 HUMCD19A 2 124 123 HUMCD19A 3 68 63 HUMCD19A 4 242 HUMCD19A 4 407 HUMCD19A 4 669 HUMCD19A 4 943 HUMCD19A 4 1760 HUMCD19A 4 1885 69 HUMCD19A 5 275 54 D88010 2 72 157 D88010 3 329 D88010 3 505 D88010 3 720 D88010 3 1124 D88010 3 1158 D88010 3 1523 21 D88010 4 209 7 D88010 5 291 2 HUMRPS6B 1 3 HUMRPS6B 1 39 HUMRPS6B 1 424 22 HUMRPS6B 2 23 HUMRPS6B 2 54 HUMRPS6B 2 108 HUMRPS6B 2 483 136 HUMRPS6B 4 37 HUMRPS6B 4 270 HUMRPS6B 4 754 HUMRPS6B 4 865 75 D89060 2 811 D89060 2 819 D89060 2 889 D89060 2 1352 D89060 2 1371 D89060 2 1472 D89060 2 1507 D89060 2 1729 D89060 2 1911 D89060 2 2120 D89060 2 2131 D89060 2 2161 D89060 2 2341 D89060 2 2549 D89060 2 2553 D89060 2 2625 D89060 2 2713 D89060 2 2812 D89060 2 3135 D89060 2 3144 D89060 2 4349 D89060 2 4401 D89060 2 4595 183 D89060 3 299 210 D89060 5 3 D89060 5 97 D89060 5 348 D89060 5 420 D89060 5 428 D89060 5 551 2 D89060 6 133 19 D89060 7 408 2 D89060 8 144 D89060 8 205 D89060 8 292 49 D89060 10 9 HSU95012 1 306 HSU95012 1 631 HSU95012 1 787 136 HSINT1G 1 3 2 HSINT1G 2 494 204 HSINT1G 3 71 HSINT1G 3 169 HSINT1G 3 410 64 HSU25816 1 15 HSU25816 1 56 18 HSU25816 3 18 2 HSCKIIBE 1 803 283 HSCKIIBE 2 366 HSCKIIBE 2 452 HSCKIIBE 2 465 102 HSCKIIBE 4 93 HSCKIIBE 4 98 9 HSCKIIBE 5 244 HSCKIIBE 5 252 HSCKIIBE 5 264 2 HUMEMBPA 1 292 HUMEMBPA 1 492 54 HUMEMBPA 2 25 HUMEMBPA 2 139 HUMEMBPA 2 246 91 HUMEMBPA 3 224 HUMEMBPA 3 325 13 HUMEMBPA 4 4 HUMTS1 1 179 HUMTS1 1 221 HUMTS1 1 794 HUMTS1 1 862 HUMTS1 1 1184 96 HUMTS1 2 23 HUMTS1 2 84 HUMTS1 2 143 HUMTS1 2 217 HUMTS1 2 509 HUMTS1 2 688 HUMTS1 2 923 HUMTS1 2 950 HUMTS1 2 1069 HUMTS1 2 1639 HUMTS1 2 1850 HUMTS1 2 2053 HUMTS1 2 2345 127 HUMTS1 3 248 HUMTS1 3 315 HUMTS1 3 946 HUMTS1 3 1470 HUMTS1 3 1912 HUMTS1 3 1924 HUMTS1 3 1949 HUMTS1 3 2235 HUMTS1 3 2654 HUMTS1 3 2830 HUMTS1 3 2975 HUMTS1 3 3370 HUMTS1 3 3623 HUMTS1 3 3825 HUMTS1 3 4258 HUMTS1 3 4941 HUMTS1 3 4955 HUMTS1 3 4994 HUMTS1 3 5346 HUMTS1 3 5708 HUMTS1 3 5740 HUMTS1 3 5777 HUMTS1 3 6001 HUMTS1 3 6180 HUMTS1 3 6235 72 HUMTS1 4 633 HUMTS1 4 717 HUMTS1 4 956 3 HUMTS1 5 18 HUMTS1 5 115 HUMTS1 5 119 58 HUMTS1 6 66 HUMTS1 6 146 HUMTS1 6 452 HUMTS1 6 742 HUMTS1 6 811 HUMTS1 6 870 43 HSNFLG 1 158 HSNFLG 1 498 103 HSNFLG 2 348 2 HSNFLG 3 61 HSNFLG 3 172 HSNFLG 3 221 57 HSU19906 1 564 HSU19906 1 1005 HSU19906 1 1057 HSU19906 1 1318 HSU19906 1 1477 HSU19906 1 1513 102 AF016052 2 1317 AF016052 2 1340 AF016052 2 1655 33 HSU61537 1 162 HSU61537 1 387 HSU61537 1 1445 5 HSU61537 2 44 HSU61537 2 446 HSU61537 2 949 HSU61537 2 1086 HSU61537 2 1229 HSU61537 2 1274 HSU61537 2 1416 HSU61537 2 1511 HSU61537 2 1687 HSU61537 2 1698 HSU61537 2 2054 HSU61537 2 2266 HSU61537 2 2298 HSU61537 2 2319 HSU61537 2 2627 HSU61537 2 2908 HSU61537 2 3556 HSU61537 2 3808 HSU61537 2 3988 HSU61537 2 4081 HSU61537 2 4453 HSU61537 2 4470 85 HUMATPSAS 1 290 HUMATPSAS 1 333 HUMATPSAS 1 378 HUMATPSAS 1 439 HUMATPSAS 1 502 HUMATPSAS 1 882 HUMATPSAS 1 1064 HUMATPSAS 1 1267 HUMATPSAS 1 1403 HUMATPSAS 1 1883 HUMATPSAS 1 2028 HUMATPSAS 1 2189 HUMATPSAS 1 2276 HUMATPSAS 1 2409 HUMATPSAS 1 2592 HUMATPSAS 1 2894 HUMATPSAS 1 2951 328 HUMATPSAS 2 72 HUMATPSAS 2 275 HUMATPSAS 2 341 HUMATPSAS 2 841 HUMATPSAS 2 867 HUMATPSAS 2 1040 HUMATPSAS 2 1175 HUMATPSAS 2 1323 HUMATPSAS 2 1999 HUMATPSAS 2 3098 36 HUMATPSAS 3 382 HUMATPSAS 3 440 HUMATPSAS 3 724 HUMATPSAS 3 963 HUMATPSAS 3 994 HUMATPSAS 3 1196 HUMATPSAS 3 1566 37 HUMATPSAS 5 75 HUMATPSAS 5 183 HUMATPSAS 5 291 HUMATPSAS 5 309 HUMATPSAS 5 526 2 HUMATPSAS 6 132 HUMATPSAS 6 353 HUMATPSAS 6 446 HUMATPSAS 6 526 HUMATPSAS 6 547 36 HUMATPSAS 8 370 10 HUMATPSAS 10 304 HUMATPSAS 10 397 HUMATPSAS 10 440 HUMATPSAS 10 950 HUMATPSAS 10 952 HUMATPSAS 10 1109 HUMATPSAS 10 1319 HUMATPSAS 10 1378 162 HUMATPSAS 11 104 HSU23853 2 121 HSU23853 2 220 HSU23853 2 230 HSU23853 2 265 61 HSLCATG 1 269 HSLCATG 1 360 HSLCATG 1 598 HSLCATG 1 637 HSLCATG 1 644 HSLCATG 1 680 21 HSLCATG 5 34 HSLCATG 5 230 HSLCATG 5 1141 HSLCATG 5 1318 HSLCATG 5 1625 21 D63789 1 47 D63789 1 225 D63789 1 235 D63789 1 403 D63789 1 510 D63789 1 765 D63789 1 855 D63789 1 1748 21 D63789 2 29 D63789 2 87 D63789 2 91 2 HUMCD7AA 3 241 HUMCD7AA 3 243 HUMCD7AA 3 270 HUMCD7AA 3 346 52 HSMTIXG 1 120 69 HSMTIXG 2 155 HSMTIXG 2 324 HSMTIXG 2 535 HSMTIXG 2 677 45 HSPCK1 1 410 HSPCK1 1 414 HSPCK1 1 566 HSPCK1 1 844 2 HSPCK1 2 324 HSPCK1 2 663 HSPCK1 2 936 HSPCK1 2 998 2 HSPCK1 4 235 183 HSPCK1 5 10 13 HSPCK1 6 193 63 HSPCK1 7 17 HSPCK1 7 539 HSPCK1 7 614 HSPCK1 7 1494 HSPCK1 7 1715 HSPCK1 7 1779 HSPCK1 7 1797 HSPCK1 7 1879 HSPCK1 7 1916 HSPCK1 7 2246 HSPCK1 7 2473 HSPCK1 7 2477 90 HSPCK1 8 120 51 AF036329 2 8 AF036329 2 363 AF036329 2 411 AF036329 2 543 AF036329 2 562 106 HUMANT1 1 628 379 HUMANT1 2 136 HUMANT1 2 404 87 HUMANT1 3 230 HUMANT1 3 602 108 HUMETMAGA 1 13 HUMETMAGA 1 97 162 D85429 1 547 D85429 1 815 D85429 1 854 303 D85429 2 11 D85429 2 84 D85429 2 91 28 HUMCKMT 1 39 HUMCKMT 1 54 HUMCKMT 1 66 HUMCKMT 1 538 2 HUMCKMT 3 118 HUMCKMT 3 193 121 HUMCKMT 6 27 HUMCKMT 6 72 HUMCKMT 6 285 HUMCKMT 6 315 HUMCKMT 6 320 HUMCKMT 6 418 HUMCKMT 6 871 HUMCKMT 6 890 HUMCKMT 6 966 40 HUMCKMT 7 28 HUMCKMT 7 42 HUMCKMT 7 275 HUMCKMT 7 443 31 HUMCKMT 8 60 HUMCKMT 8 139 10 HUMADPRF02 1 278 180 HUMADPRF02 2 147 60 HUMADPRF02 3 286 HUMADPRF02 3 382 109 HSHNRNPA 1 53 HSHNRNPA 1 271 7 HSHNRNPA 5 29 15 HSHNRNPA 7 57 HSHNRNPA 7 203 HSHNRNPA 7 359 HSHNRNPA 7 732 HSHNRNPA 7 903 21 HSHNRNPA 8 12 15 HUMATPGG 4 202 HUMATPGG 4 227 HUMATPGG 4 259 HUMATPGG 4 347 HUMATPGG 4 490 HUMATPGG 4 1013 HUMATPGG 4 1386 HUMATPGG 4 1436 100 HUMATPGG 7 319 HUMATPGG 7 574 229 HUMATPGG 8 72 57 HUMATPGG 11 31 HUMATPGG 11 428 HUMATPGG 11 451 HUMATPGG 11 466 189 HUMATPGG 12 1005 HUMATPGG 12 1072 31 HUMATPGG 16 163 HUMATPGG 16 215 HUMATPGG 16 287 HUMATPGG 16 433 HUMATPGG 16 598 HUMATPGG 16 670 130 HUMATPGG 17 29 156 HUMATPGG 18 1061 94 HUMTPALBU 1 264 184 HUMTPALBU 2 86 HUMTPALBU 2 156 HUMTPALBU 2 291 2 HUMTPALBU 3 190 HUMTPALBU 3 199 168 HUMTPALBU 4 355 HUMTPALBU 4 430 129 HSCRTRGN 1 279 HSCRTRGN 1 316 HSCRTRGN 1 730 687 HSCRTRGN 2 269 HSCRTRGN 2 509 78 HSCRTRGN 3 231 HSCRTRGN 3 236 2 HSCRTRGN 4 83 397 HSCRTRGN 11 15 HSCRTRGN 12 144 40 HSARS81S 1 367 HSARS81S 1 372 36 HSARS81S 2 104 HSARS81S 2 206 HSARS81S 2 436 HSARS81S 2 441 336 HUMPAIA 1 23 HUMPAIA 1 347 HUMPAIA 1 899 HUMPAIA 1 1075 HUMPAIA 1 1250 267 HUMPAIA 2 266 HUMPAIA 2 608 HUMPAIA 2 925 HUMPAIA 2 937 102 HUMPAIA 3 420 HUMPAIA 3 438 HUMPAIA 3 510 HUMPAIA 3 925 HUMPAIA 3 998 HUMPAIA 3 1081 HUMPAIA 3 1105 HUMPAIA 3 1114 HUMPAIA 3 1529 138 HUMPAIA 4 285 HUMPAIA 4 616 HUMPAIA 4 692 HUMPAIA 4 710 HUMPAIA 4 893 HUMPAIA 4 907 HUMPAIA 4 1077 HUMPAIA 4 1531 2 HUMPAIA 6 14 HUMPAIA 6 346 HUMPAIA 6 360 HUMPAIA 6 737 HUMPAIA 6 1035 234 HUMDKERB 1 174 HUMDKERB 1 323 HUMDKERB 1 558 HUMDKERB 1 685 HUMDKERB 1 1735 HUMDKERB 1 1988 HUMDKERB 1 2249 HUMDKERB 1 2386 HUMDKERB 1 2412 283 HUMDKERB 2 463 HUMDKERB 2 608 2 HUMDKERB 3 160 HUMDKERB 3 164 HUMDKERB 3 276 HUMDKERB 3 296 HUMDKERB 3 302 85 HUMDKERB 4 190 HUMDKERB 4 271 124 HUMDKERB 5 45 HUMDKERB 5 203 HUMDKERB 5 223 HUMDKERB 5 284 58 HUMDKERB 7 231 HUMDKERB 7 253 99 HSBSF2 1 61 HSBSF2 2 281 HSBSF2 2 501 HSBSF2 2 601 HSBSF2 2 653 HSBSF2 2 862 HSBSF2 2 1017 79 HSBSF2 3 98 HSBSF2 3 102 HSBSF2 3 122 HSBSF2 3 181 HSBSF2 3 207 HSBSF2 3 587 253 HSBSF2 4 3 HSBSF2 4 233 HSBSF2 4 715 HSBSF2 4 825 HSBSF2 4 841 HSBSF2 4 903 HSBSF2 4 1113 HSBSF2 4 1341 109 HUMHBA1 1 44 HUMHBA1 1 48 2 HSGMCSFG 1 3 43 HSGMCSFG 2 53 HSGMCSFG 2 401 HSGMCSFG 2 435 HSGMCSFG 2 518 22 HSGMCSFG 3 260 HSGMCSFG 3 267 HSGMCSFG 3 643 HSGMCSFG 3 672 HSGMCSFG 3 680 43 HUMTKRA 2 465 HUMTKRA 2 499 HUMTKRA 2 562 HUMTKRA 2 973 HUMTKRA 2 1018 HUMTKRA 2 1036 HUMTKRA 2 1304 HUMTKRA 2 1381 2 HUMTKRA 3 130 HUMTKRA 3 194 HUMTKRA 3 911 HUMTKRA 3 915 HUMTKRA 3 1013 HUMTKRA 3 1301 HUMTKRA 3 1326 HUMTKRA 3 1477 HUMTKRA 3 2035 HUMTKRA 3 2073 62 HUMTKRA 4 430 HUMTKRA 4 752 HUMTKRA 4 827 HUMTKRA 4 1007 HUMTKRA 4 1156 HUMTKRA 4 1160 HUMTKRA 4 1256 HUMTKRA 4 1463 HUMTKRA 4 1553 HUMTKRA 4 1733 HUMTKRA 4 1825 HUMTKRA 4 2187 HUMTKRA 4 2593 HUMTKRA 4 2729 HUMTKRA 4 2842 HUMTKRA 4 3165 HUMTKRA 4 3250 HUMTKRA 4 3412 HUMTKRA 4 3633 HUMTKRA 4 4306 HUMTKRA 4 4420 HUMTKRA 4 4478 HUMTKRA 4 4757 HUMTKRA 4 4761 HUMTKRA 4 4773 HUMTKRA 4 5276 HUMTKRA 4 5281 HUMTKRA 4 5341 HUMTKRA 4 5523 HUMTKRA 4 5540 HUMTKRA 4 5729 121 HUMTKRA 5 185 HUMTKRA 5 250 HUMTKRA 5 315 34 HSU46920 1 217 HSU46920 1 611 HSU46920 1 756 115 HSU46920 2 19 HSU46920 2 29 57 HSU46920 3 3 HSU46920 3 100 HSU46920 3 708 HSU46920 3 918 31 HSU46920 5 70 28 HUMSEMI 1 12 HUMSEMI 1 181 15 HUMADAG 1 436 HUMADAG 1 456 HUMADAG 1 558 HUMADAG 1 752 HUMADAG 1 833 HUMADAG 1 835 HUMADAG 1 984 HUMADAG 1 1076 HUMADAG 1 1166 HUMADAG 1 1202 HUMADAG 1 1213 HUMADAG 1 1276 HUMADAG 1 1507 HUMADAG 1 1592 HUMADAG 1 2091 HUMADAG 1 2127 HUMADAG 1 3119 HUMADAG 1 3503 HUMADAG 1 3873 HUMADAG 1 3915 HUMADAG 1 4220 HUMADAG 1 4356 HUMADAG 1 5027 HUMADAG 1 5464 HUMADAG 1 6032 HUMADAG 1 6074 HUMADAG 1 6178 HUMADAG 1 6912 HUMADAG 1 7125 HUMADAG 1 7503 HUMADAG 1 7624 HUMADAG 1 7698 HUMADAG 1 7760 HUMADAG 1 8007 HUMADAG 1 8370 HUMADAG 1 8433 HUMADAG 1 9122 HUMADAG 1 9351 HUMADAG 1 9393 HUMADAG 1 9438 HUMADAG 1 9456 HUMADAG 1 9770 HUMADAG 1 10385 HUMADAG 1 10684 HUMADAG 1 10768 HUMADAG 1 10825 HUMADAG 1 10911 HUMADAG 1 11004 HUMADAG 1 11330 HUMADAG 1 11596 HUMADAG 1 11792 HUMADAG 1 11810 HUMADAG 1 11890 HUMADAG 1 12043 HUMADAG 1 12960 HUMADAG 1 13002 HUMADAG 1 13096 HUMADAG 1 13140 HUMADAG 1 13310 HUMADAG 1 13336 HUMADAG 1 13785 HUMADAG 1 14400 HUMADAG 1 14417 HUMADAG 1 15113 223 HUMADAG 2 236 HUMADAG 2 288 HUMADAG 2 411 HUMADAG 2 647 HUMADAG 2 952 HUMADAG 2 1483 HUMADAG 2 1619 HUMADAG 2 1713 HUMADAG 2 1821 HUMADAG 2 3052 HUMADAG 2 3299 HUMADAG 2 3442 HUMADAG 2 3454 HUMADAG 2 3819 HUMADAG 2 4431 HUMADAG 2 4515 HUMADAG 2 4793 HUMADAG 2 4931 HUMADAG 2 5352 HUMADAG 2 5459 HUMADAG 2 5960 HUMADAG 2 6239 HUMADAG 2 6759 2 HUMADAG 3 135 HUMADAG 3 181 HUMADAG 3 738 HUMADAG 3 1180 HUMADAG 3 1615 HUMADAG 3 1631 HUMADAG 3 1894 HUMADAG 3 2244 HUMADAG 3 2342 2 HUMADAG 4 366 HUMADAG 4 651 2 HUMADAG 5 257 HUMADAG 5 826 HUMADAG 5 920 HUMADAG 5 1175 6 HUMADAG 6 37 HUMADAG 6 110 HUMADAG 6 339 HUMADAG 6 938 40 HUMADAG 9 426 HUMADAG 9 709 HUMADAG 9 1035 HUMADAG 9 1391 2 HUMADAG 10 93 HUMADAG 10 257 HUMADAG 10 349 28 HUMBNPA 1 181 HUMBNPA 1 192 94 HUMBNPA 2 457 HUMBNPA 2 476 99 AF015954 1 198 154 AF015954 2 268 AF015954 2 422 AF015954 2 501 AF015954 2 1027 51 AF015954 3 518 24 HUMAZCDI 1 210 39 HUMAZCDI 2 85 HUMAZCDI 2 89 HUMAZCDI 2 574 2 HUMAZCDI 3 168 HUMAZCDI 3 230 HUMAZCDI 3 278 HUMAZCDI 3 283 HUMAZCDI 3 323 HUMAZCDI 3 339 HUMAZCDI 3 671 22 HUMAZCDI 4 339 43 HSU37022 1 55 HSU37022 1 135 2 HSU37022 2 26 HSU37022 2 67 22 HSU37022 6 227 HSU37022 6 245 55 HSACTH 1 148 HSACTH 1 434 HSACTH 1 642 HSACTH 1 765 HSACTH 1 1142 HSACTH 1 1225 HSACTH 1 1344 HSACTH 1 1860 HSACTH 1 1880 HSACTH 1 2450 HSACTH 1 2623 HSACTH 1 2714 13 HSIL05 2 93 HSIL05 2 400 HSIL05 2 581 HSIL05 2 585 HSIL05 2 622 HSIL05 2 840 HSIL05 2 918 HSIL05 2 1185 HSIL05 2 1567 HSIL05 2 1932 HSIL05 2 2077 HSIL05 2 2109 34 HSIL05 3 111 HSIL05 3 281 HSIL05 3 581 HSIL05 3 702 HSIL05 3 1295 HSIL05 3 1733 HSIL05 3 1753 HSIL05 3 1815 79 HSGCAP2 1 154 HSGCAP2 1 256 HSGCAP2 1 357 HSGCAP2 1 685 HSGCAP2 1 776 HSGCAP2 1 898 31 HSGCAP2 2 110 HSGCAP2 2 161 HSGCAP2 2 477 78 HSNFM 1 420 322 HSNFM 2 15 HSNFM 2 746 HSNFM 2 896 HSNFM 2 1075 HSNFM 2 1096 HSNFM 2 1173 HSNFM 2 1221 HSNFM 2 1241 149 HUMCOL2A1Z 1 406 HUMCOL2A1Z 1 888 HUMCOL2A1Z 1 920 HUMCOL2A1Z 1 1054 HUMCOL2A1Z 1 1828 HUMCOL2A1Z 1 2302 HUMCOL2A1Z 1 2808 HUMCOL2A1Z 1 3328 HUMCOL2A1Z 1 3586 HUMCOL2A1Z 1 3808 HUMCOL2A1Z 1 3871 HUMCOL2A1Z 1 3894 255 HUMCOL2A1Z 2 256 HUMCOL2A1Z 2 412 HUMCOL2A1Z 2 695 HUMCOL2A1Z 2 745 HUMCOL2A1Z 2 829 HUMCOL2A1Z 2 911 HUMCOL2A1Z 2 963 HUMCOL2A1Z 2 1075 HUMCOL2A1Z 2 1412 HUMCOL2A1Z 2 1437 30 HUMCOL2A1Z 7 275 HUMCOL2A1Z 7 428 HUMCOL2A1Z 7 833 HUMCOL2A1Z 7 853 55 HUMCOL2A1Z 10 349 43 HUMCOL2A1Z 11 57 HUMCOL2A1Z 11 98 HUMCOL2A1Z 11 481 HUMCOL2A1Z 11 554 HUMCOL2A1Z 11 650 16 HUMCOL2A1Z 12 85 37 HUMCOL2A1Z 13 12 HUMCOL2A1Z 13 64 HUMCOL2A1Z 15 272 HUMCOL2A1Z 15 512 112 HUMCOL2A1Z 16 55 HUMCOL2A1Z 16 237 HUMCOL2A1Z 16 373 HUMCOL2A1Z 16 519 HUMCOL2A1Z 16 573 HUMCOL2A1Z 16 649 HUMCOL2A1Z 16 1956 HUMCOL2A1Z 16 2565 HUMCOL2A1Z 16 2627 HUMCOL2A1Z 16 2705 10 HUMCOL2A1Z 17 23 43 HUMCOL2A1Z 18 190 HUMCOL2A1Z 18 702 HUMCOL2A1Z 18 794 HUMCOL2A1Z 18 1121 HUMCOL2A1Z 18 1280 HUMCOL2A1Z 18 1460 103 HUMCOL2A1Z 19 244 58 HUMCOL2A1Z 22 483 46 HUMCOL2A1Z 23 4 HUMCOL2A1Z 23 281 HUMCOL2A1Z 23 285 7 HUMCOL2A1Z 27 149 85 HUMCOL2A1Z 28 268 25 HUMCOL2A1Z 29 93 112 HUMCOL2A1Z 30 3 241 HUMCOL2A1Z 33 3 52 HUMCOL2A1Z 35 3 HUMCOL2A1Z 35 162 43 HUMCOL2A1Z 37 199 HUMCOL2A1Z 37 325 202 HUMCOL2A1Z 40 143 226 HUMCOL2A1Z 41 503 HUMCOL2A1Z 41 569 HUMCOL2A1Z 41 706 100 HUMCOL2A1Z 42 45 79 HUMCOL2A1Z 43 105 HUMCOL2A1Z 44 48 HUMCOL2A1Z 44 215 HUMCOL2A1Z 44 239 HUMCOL2A1Z 44 243 HUMCOL2A1Z 44 306 HUMCOL2A1Z 45 60 HUMCOL2A1Z 47 66 HUMCOL2A1Z 51 192 195 HUMCOL2A1Z 52 163 19 HUMCOL2A1Z 53 153 58 HUMCYPIIE 1 50 HUMCYPIIE 1 54 HUMCYPIIE 1 631 HUMCYPIIE 1 837 232 HUMCYPIIE 2 351 HUMCYPIIE 2 909 HUMCYPIIE 2 1956 HUMCYPIIE 2 2494 HUMCYPIIE 2 2575 HUMCYPIIE 2 2654 96 HUMCYPIIE 3 119 HUMCYPIIE 3 197 HUMCYPIIE 3 321 192 HUMCYPIIE 5 614 HUMCYPIIE 5 718 HUMCYPIIE 5 815 148 HUMCYPIIE 6 7 HUMCYPIIE 6 119 HUMCYPIIE 6 335 HUMCYPIIE 6 363 HUMCYPIIE 6 423 HUMCYPIIE 6 539 HUMCYPIIE 6 560 HUMCYPIIE 6 609 HUMCYPIIE 6 614 HUMCYPIIE 6 783 HUMCYPIIE 6 1093 HUMCYPIIE 6 1222 HUMCYPIIE 6 1544 HUMCYPIIE 6 2224 HUMCYPIIE 6 2498 HUMCYPIIE 6 2558 HUMCYPIIE 6 2606 HUMCYPIIE 6 2638 HUMCYPIIE 6 2642 HUMCYPIIE 6 2729 102 HUMCYPIIE 8 217 HUMCYPIIE 8 416 HUMCYPIIE 8 755 96 HSAPC3A 2 67 HSAPC3A 2 650 HSAPC3A 2 961 HSAPC3A 2 1146 HSAPC3A 2 1194 HSAPC3A 2 1336 HSAPC3A 2 1391 HSAPC3A 2 1599 245 HUMRETBLAS 1 1277 HUMRETBLAS 1 1921 HUMRETBLAS 1 2256 HUMRETBLAS 1 2490 HUMRETBLAS 1 2604 HUMRETBLAS 1 2778 HUMRETBLAS 1 3162 2 HUMRETBLAS 2 220 HUMRETBLAS 2 707 HUMRETBLAS 2 809 HUMRETBLAS 2 846 HUMRETBLAS 2 1019 HUMRETBLAS 2 1031 HUMRETBLAS 2 1143 HUMRETBLAS 2 1696 HUMRETBLAS 2 1936 HUMRETBLAS 2 2609 HUMRETBLAS 2 2646 HUMRETBLAS 2 2945 HUMRETBLAS 2 2949 HUMRETBLAS 2 3497 HUMRETBLAS 2 3561 HUMRETBLAS 2 3585 HUMRETBLAS 2 3730 HUMRETBLAS 2 3974 HUMRETBLAS 2 4138 HUMRETBLAS 2 4655 HUMRETBLAS 2 5883 HUMRETBLAS 2 6153 HUMRETBLAS 2 6487 HUMRETBLAS 2 6724 HUMRETBLAS 2 6792 HUMRETBLAS 2 7066 HUMRETBLAS 2 7165 HUMRETBLAS 2 7183 HUMRETBLAS 2 7897 HUMRETBLAS 2 8168 HUMRETBLAS 2 8283 HUMRETBLAS 2 9972 HUMRETBLAS 2 10761 HUMRETBLAS 2 11041 HUMRETBLAS 2 13180 HUMRETBLAS 2 14204 HUMRETBLAS 2 14917 HUMRETBLAS 2 15908 HUMRETBLAS 2 15976 HUMRETBLAS 2 16006 HUMRETBLAS 2 16123 HUMRETBLAS 2 16521 HUMRETBLAS 2 17013 HUMRETBLAS 2 17017 HUMRETBLAS 2 17180 HUMRETBLAS 2 17581 HUMRETBLAS 2 17765 HUMRETBLAS 2 18342 HUMRETBLAS 2 18423 HUMRETBLAS 2 19003 HUMRETBLAS 2 19044 HUMRETBLAS 2 19102 HUMRETBLAS 2 19480 HUMRETBLAS 2 19489 HUMRETBLAS 2 19658 HUMRETBLAS 2 19992 HUMRETBLAS 2 20247 HUMRETBLAS 2 21202 HUMRETBLAS 2 21495 HUMRETBLAS 2 21846 HUMRETBLAS 2 21917 HUMRETBLAS 2 21985 HUMRETBLAS 2 22024 HUMRETBLAS 2 22296 HUMRETBLAS 2 23257 HUMRETBLAS 2 23410 HUMRETBLAS 2 23945 HUMRETBLAS 2 24185 HUMRETBLAS 2 24197 HUMRETBLAS 2 24205 HUMRETBLAS 2 24312 HUMRETBLAS 2 24474 HUMRETBLAS 2 24552 HUMRETBLAS 2 24607 HUMRETBLAS 2 24751 HUMRETBLAS 2 25020 HUMRETBLAS 2 25271 HUMRETBLAS 2 25531 HUMRETBLAS 2 25535 HUMRETBLAS 2 25775 HUMRETBLAS 2 26039 HUMRETBLAS 2 26183 HUMRETBLAS 2 26187 HUMRETBLAS 2 26250 HUMRETBLAS 2 26804 HUMRETBLAS 2 26961 HUMRETBLAS 2 26989 HUMRETBLAS 2 27301 HUMRETBLAS 2 27773 HUMRETBLAS 2 28172 HUMRETBLAS 2 28296 HUMRETBLAS 2 28867 HUMRETBLAS 2 28986 HUMRETBLAS 2 29035 HUMRETBLAS 2 29435 HUMRETBLAS 2 29833 HUMRETBLAS 2 30212 HUMRETBLAS 2 30585 HUMRETBLAS 2 30920 HEMRETBLAS 2 30925 HUMRETBLAS 2 31139 HUMRETBLAS 2 31253 HUMRETBLAS 2 31331 HUMRETBLAS 2 31339 HUMRETBLAS 2 31965 HUMRETBLAS 2 32186 HUMRETBLAS 2 32190 HUMRETBLAS 2 33074 HUMRETBLAS 2 33124 HUMRETBLAS 2 33128 76 HUMRETBLAS 3 357 49 HUMRETBLAS 3 365 HUMRETBLAS 3 486 HUMRETBLAS 3 642 HUMRETBLAS 3 1313 HUMRETBLAS 3 1386 HUMRETBLAS 3 1596 HUMRETBLAS 3 1658 HUMRETBLAS 3 1754 HUMRETBLAS 3 1759 HUMRETBLAS 3 1831 HUMRETBLAS 3 1943 HUMRETBLAS 3 2174 HUMRETBLAS 3 2193 HUMRETBLAS 3 2224 HUMRETBLAS 3 2326 2 HUMRETBLAS 4 90 HUMRETBLAS 4 94 HUMRETBLAS 4 1172 HUMRETBLAS 4 1976 HUMRETBLAS 4 1988 HUMRETBLAS 4 2167 HUMRETBLAS 4 2361 HUMRETBLAS 4 2450 2 HUMRETBLAS 5 79 HUMRETBLAS 5 569 HUMRETBLAS 5 693 HUMRETBLAS 5 708 HUMRETBLAS 5 980 2 HUMRETBLAS 6 651 HUMRETBLAS 6 922 HUMRETBLAS 6 1343 HUMRETBLAS 6 1518 HUMRETBLAS 6 1605 HUMRETBLAS 6 1791 HUMRETBLAS 6 2350 HUMRETBLAS 6 2745 HUMRETBLAS 6 2787 HUMRETBLAS 6 2880 HUMRETBLAS 6 3117 HUMRETBLAS 6 3550 HUMRETBLAS 6 3635 HUMRETBLAS 6 3958 HUMRETBLAS 6 3969 HUMRETBLAS 6 4776 HUMRETBLAS 6 6337 HUMRETBLAS 6 6445 HUMRETBLAS 6 6539 HUMRETBLAS 6 6560 HUMRETBLAS 6 6577 HUMRETBLAS 6 6915 HUMRETBLAS 6 6978 HUMRETBLAS 6 7194 HUMRETBLAS 6 7523 HUMRETBLAS 6 7649 HUMRETBLAS 6 8712 HUMRETBLAS 6 8745 HUMRETBLAS 6 8906 HUMRETBLAS 6 9339 HUMRETBLAS 6 9448 HUMRETBLAS 6 10060 HUMRETBLAS 6 10183 27 HUMRETBLAS 7 136 HUMRETBLAS 7 612 HUMRETBLAS 7 718 HUMRETBLAS 7 1129 HUMRETBLAS 7 1195 HUMRETBLAS 7 1278 HUMRETBLAS 7 1756 60 HUMRETBLAS 8 47 HUMRETBLAS 8 272 HUMRETBLAS 8 1561 HUMRETBLAS 8 1647 HUMRETBLAS 8 1722 7 HUMRETBLAS 9 332 HUMRETBLAS 9 582 HUMRETBLAS 9 993 HUMRETBLAS 9 998 HUMRETBLAS 9 1109 HUMRETBLAS 9 1364 HUMRETBLAS 9 1385 HUMRETBLAS 9 1689 HUMRETBLAS 9 1918 HUMRETBLAS 9 1932 HUMRETBLAS 9 2016 7 HUMRETBLAS 10 57 HUMRETBLAS 10 188 HUMRETBLAS 10 274 HUMRETBLAS 10 895 20 HUMRETBLAS 11 99 HUMRETBLAS 11 124 HUMRETBLAS 11 187 HUMRETBLAS 11 267 HUMRETBLAS 11 866 HUMRETBLAS 11 1424 HUMRETBLAS 11 1605 HUMRETBLAS 11 2015 HUMRETBLAS 11 2604 HUMRETBLAS 11 2686 HUMRETBLAS 11 3250 HUMRETBLAS 11 3269 HUMRETBLAS 11 3331 HUMRETBLAS 11 3360 HUMRETBLAS 11 3821 HUMRETBLAS 11 4330 HUMRETBLAS 11 4638 20 HUMRETBLAS 12 1023 HUMRETBLAS 12 1800 HUMRETBLAS 12 2320 HUMRETBLAS 12 2775 HUMRETBLAS 12 3114 13 HUMRETBLAS 13 156 HUMRETBLAS 13 335 HUMRETBLAS 13 415 HUMRETBLAS 13 864 HUMRETBLAS 13 923 HUMRETBLAS 13 1020 HUMRETBLAS 13 1036 HUMRETBLAS 13 1729 HUMRETBLAS 13 1904 HUMRETBLAS 13 1986 HUMRETBLAS 13 2109 HUMRETBLAS 13 2259 HUMRETBLAS 13 2316 HUMRETBLAS 13 2323 7 HUMRETBLAS 14 79 7 HUMRETBLAS 15 44 2 HUMRETBLAS 16 53 HUMRETBLAS 16 137 HUMRETBLAS 16 254 21 HUMRETBLAS 17 67 HUMRETBLAS 17 307 HUMRETBLAS 17 1432 HUMRETBLAS 17 1535 HUMRETBLAS 17 2037 HUMRETBLAS 17 2061 HUMRETBLAS 17 2311 HUMRETBLAS 17 2343 HUMRETBLAS 17 2436 HUMRETBLAS 17 3060 HUMRETBLAS 17 3582 HUMRETBLAS 17 3664 HUMRETBLAS 17 3792 HUMRETBLAS 17 3819 HUMRETBLAS 17 3929 HUMRETBLAS 17 4058 HUMRETBLAS 17 4071 HUMRETBLAS 17 4487 HUMRETBLAS 17 4529 HUMRETBLAS 17 4619 HUMRETBLAS 17 4655 HUMRETBLAS 17 4982 HUMRETBLAS 17 5135 HUMRETBLAS 17 5165 HUMRETBLAS 17 5335 HUMRETBLAS 17 5425 HUMRETBLAS 17 5606 HUMRETBLAS 17 5688 HUMRETBLAS 17 6102 HUMRETBLAS 17 6253 HUMRETBLAS 17 6269 HUMRETBLAS 17 6332 HUMRETBLAS 17 6902 HUMRETBLAS 17 6912 HUMRETBLAS 17 6949 HUMRETBLAS 17 7045 HUMRETBLAS 17 7086 HUMRETBLAS 17 7485 HUMRETBLAS 17 7579 HUMRETBLAS 17 7791 HUMRETBLAS 17 8011 HUMRETBLAS 17 8057 HUMRETBLAS 17 8221 HUMRETBLAS 17 8476 HUMRETBLAS 17 8565 HUMRETBLAS 17 9018 HUMRETBLAS 17 9192 HUMRETBLAS 17 9408 HUMRETBLAS 17 9507 HUMRETBLAS 17 10891 HUMRETBLAS 17 11063 HUMRETBLAS 17 11272 HUMRETBLAS 17 11349 HUMRETBLAS 17 12127 HUMRETBLAS 17 12325 HUMRETBLAS 17 12563 HUMRETBLAS 17 12587 HUMRETBLAS 17 13099 HUMRETBLAS 17 13457 HUMRETBLAS 17 13550 HUMRETBLAS 17 13804 HUMRETBLAS 17 13947 HUMRETBLAS 17 14025 HUMRETBLAS 17 15362 HUMRETBLAS 17 16441 HUMRETBLAS 17 16550 HUMRETBLAS 17 16884 HUMRETBLAS 17 17146 HUMRETBLAS 17 17336 HUMRETBLAS 17 17371 HUMRETBLAS 17 17563 HUMRETBLAS 17 17664 HUMRETBLAS 17 17692 HUMRETBLAS 17 17703 HUMRETBLAS 17 17802 HUMRETBLAS 17 18045 HUMRETBLAS 17 18149 HUMRETBLAS 17 18246 HUMRETBLAS 17 18323 HUMRETBLAS 17 18615 HUMRETBLAS 17 18722 HUMRETBLAS 17 18755 HUMRETBLAS 17 18997 HUMRETBLAS 17 19061 HUMRETBLAS 17 19199 HUMRETBLAS 17 19622 HUMRETBLAS 17 20232 HUMRETBLAS 17 20251 HUMRETBLAS 17 21055 HUMRETBLAS 17 21065 HUMRETBLAS 17 21291 HUMRETBLAS 17 21315 HUMRETBLAS 17 22295 HUMRETBLAS 17 22871 HUMRETBLAS 17 22906 HUMRETBLAS 17 23344 HUMRETBLAS 17 23423 HUMRETBLAS 17 24384 HUMRETBLAS 17 24591 HUMRETBLAS 17 24659 HUMRETBLAS 17 24663 HUMRETBLAS 17 24667 HUMRETBLAS 17 24671 HUMRETBLAS 17 24682 HUMRETBLAS 17 24719 HUMRETBLAS 17 24746 HUMRETBLAS 17 24758 HUMRETBLAS 17 24793 HUMRETBLAS 17 25164 HUMRETBLAS 17 25280 HUMRETBLAS 17 25365 HUMRETBLAS 17 25673 HUMRETBLAS 17 25848 HUMRETBLAS 17 25871 HUMRETBLAS 17 25911 HUMRETBLAS 17 25941 HUMRETBLAS 17 26193 HUMRETBLAS 17 26272 HUMRETBLAS 17 26848 HUMRETBLAS 17 27069 HUMRETBLAS 17 27589 HUMRETBLAS 17 27651 HUMRETBLAS 17 28395 HUMRETBLAS 17 28581 HUMRETBLAS 17 28884 HUMRETBLAS 17 28926 HUMRETBLAS 17 28957 HUMRETBLAS 17 29117 HUMRETBLAS 17 29536 HUMRETBLAS 17 29652 HUMRETBLAS 17 29905 HUMRETBLAS 17 29966 HUMRETBLAS 17 30699 HUMRETBLAS 17 30796 HUMRETBLAS 17 31538 HUMRETBLAS 17 32006 HUMRETBLAS 17 32657 HUMRETBLAS 17 32937 HUMRETBLAS 17 32948 HUMRETBLAS 17 32964 HUMRETBLAS 17 33133 HUMRETBLAS 17 33403 HUMRETBLAS 17 33407 HUMRETBLAS 17 34210 HUMRETBLAS 17 34454 HUMRETBLAS 17 34496 HUMRETBLAS 17 34573 HUMRETBLAS 17 34733 HUMRETBLAS 17 34737 HUMRETBLAS 17 35316 HUMRETBLAS 17 35630 HUMRETBLAS 17 35724 HUMRETBLAS 17 35977 HUMRETBLAS 17 36175 HUMRETBLAS 17 36822 HUMRETBLAS 17 37378 HUMRETBLAS 17 38065 HUMRETBLAS 17 39487 HUMRETBLAS 17 39912 HUMRETBLAS 17 40220 HUMRETBLAS 17 41552 HUMRETBLAS 17 41595 HUMRETBLAS 17 41658 HUMRETBLAS 17 42232 HUMRETBLAS 17 42553 HUMRETBLAS 17 42806 HUMRETBLAS 17 42868 HUMRETBLAS 17 43053 HUMRETBLAS 17 43358 HUMRETBLAS 17 43431 HUMRETBLAS 17 43973 HUMRETBLAS 17 43983 HUMRETBLAS 17 44065 HUMRETBLAS 17 44102 HUMRETBLAS 17 44139 HUMRETBLAS 17 44440 HUMRETBLAS 17 44548 HUMRETBLAS 17 44989 HUMRETBLAS 17 45259 HUMRETBLAS 17 45337 HUMRETBLAS 17 45427 HUMRETBLAS 17 45670 HUMRETBLAS 17 45723 HUMRETBLAS 17 45776 HUMRETBLAS 17 45829 HUMRETBLAS 17 45882 HUMRETBLAS 17 45935 HUMRETBLAS 17 45988 HUMRETBLAS 17 46041 HUMRETBLAS 17 46094 HUMRETBLAS 17 46147 HUMRETBLAS 17 46200 HUMRETBLAS 17 46253 HUMRETBLAS 17 46306 HUMRETBLAS 17 46359 HUMRETBLAS 17 46412 HUMRETBLAS 17 46465 HUMRETBLAS 17 46518 HUMRETBLAS 17 46571 HUMRETBLAS 17 46624 HUMRETBLAS 17 46677 HUMRETBLAS 17 46730 HUMRETBLAS 17 46783 HUMRETBLAS 17 46836 HUMRETBLAS 17 46889 HUMRETBLAS 17 46942 HUMRETBLAS 17 46995 HUMRETBLAS 17 47048 HUMRETBLAS 17 47101 HUMRETBLAS 17 47154 HUMRETBLAS 17 47207 HUMRETBLAS 17 47288 HUMRETBLAS 17 47981 HUMRETBLAS 17 48051 HUMRETBLAS 17 49244 HUMRETBLAS 17 49258 HUMRETBLAS 17 49456 HUMRETBLAS 17 49898 HUMRETBLAS 17 50222 HUMRETBLAS 17 50404 HUMRETBLAS 17 50670 HUMRETBLAS 17 51079 HUMRETBLAS 17 51295 HUMRETBLAS 17 51806 HUMRETBLAS 17 51873 HUMRETBLAS 17 51912 HUMRETBLAS 17 51999 HUMRETBLAS 17 52439 HUMRETBLAS 17 53170 HUMRETBLAS 17 53542 HUMRETBLAS 17 53918 HUMRETBLAS 17 54653 HUMRETBLAS 17 54847 HUMRETBLAS 17 54855 HUMRETBLAS 17 54880 HUMRETBLAS 17 55456 HUMRETBLAS 17 55783 HUMRETBLAS 17 55787 HUMRETBLAS 17 56379 HUMRETBLAS 17 57385 HUMRETBLAS 17 57607 HUMRETBLAS 17 57819 HUMRETBLAS 17 58140 HUMRETBLAS 17 59298 HUMRETBLAS 17 59458 HUMRETBLAS 17 60528 HUMRETBLAS 17 60801 HUMRETBLAS 17 61241 HUMRETBLAS 17 61354 HUMRETBLAS 17 61393 HUMRETBLAS 17 61636 HUMRETBLAS 17 62274 HUMRETBLAS 17 62450 HUMRETBLAS 17 63013 HUMRETBLAS 17 63331 HUMRETBLAS 17 63336 HUMRETBLAS 17 63694 HUMRETBLAS 17 64495 HUMRETBLAS 17 64607 HUMRETBLAS 17 64825 HUMRETBLAS 17 64918 HUMRETBLAS 17 65116 HUMRETBLAS 17 65273 HUMRETBLAS 17 65363 HUMRETBLAS 17 65380 HUMRETBLAS 17 65639 HUMRETBLAS 17 65780 HUMRETBLAS 17 66225 HUMRETBLAS 17 66646 HUMRETBLAS 17 66688 HUMRETBLAS 17 66813 HUMRETBLAS 17 67190 HUMRETBLAS 17 68155 HUMRETBLAS 17 68496 HUMRETBLAS 17 69173 HUMRETBLAS 17 69199 HUMRETBLAS 17 69414 HUMRETBLAS 17 69503 HUMRETBLAS 17 69830 HUMRETBLAS 17 70242 HUMRETBLAS 17 70284 HUMRETBLAS 17 70734 HUMRETBLAS 17 70768 HUMRETBLAS 17 71524 HUMRETBLAS 17 71757 HUMRETBLAS 17 72006 HUMRETBLAS 17 72136 HUMRETBLAS 17 72163 HUMRETBLAS 17 72386 HUMRETBLAS 17 72456 HUMRETBLAS 17 72811 HUMRETBLAS 17 72892 HUMRETBLAS 17 73276 HUMRETBLAS 17 73360 HUMRETBLAS 17 73364 HUMRETBLAS 17 73379 HUMRETBLAS 17 73620 HUMRETBLAS 17 73624 HUMRETBLAS 17 74082 HUMRETBLAS 17 74632 HUMRETBLAS 17 74903 HUMRETBLAS 17 75271 HUMRETBLAS 17 75331 HUMRETBLAS 17 75452 HUMRETBLAS 17 75782 HUMRETBLAS 17 76408 HUMRETBLAS 17 76669 HUMRETBLAS 17 76720 HUMRETBLAS 17 77115 HUMRETBLAS 17 77285 HUMRETBLAS 17 78028 HUMRETBLAS 17 78433 HUMRETBLAS 17 78475 HUMRETBLAS 17 78917 HUMRETBLAS 17 78951 10 HUMRETBLAS 20 234 HUMRETBLAS 20 366 HUMRETBLAS 20 438 HUMRETBLAS 20 817 HUMRETBLAS 20 888 HUMRETBLAS 20 978 HUMRETBLAS 20 983 HUMRETBLAS 20 1062 HUMRETBLAS 20 1160 HUMRETBLAS 20 1660 HUMRETBLAS 20 1905 HUMRETBLAS 20 2135 HUMRETBLAS 20 2520 HUMRETBLAS 20 2702 HUMRETBLAS 20 2937 HUMRETBLAS 20 3192 HUMRETBLAS 20 3511 HUMRETBLAS 20 3648 HUMRETBLAS 20 3664 HUMRETBLAS 20 3692 382 HUMRETBLAS 21 3 HUMRETBLAS 21 16 HUMRETBLAS 21 57 HUMRETBLAS 21 118 HUMRETBLAS 21 184 HUMRETBLAS 21 258 HUMRETBLAS 21 478 HUMRETBLAS 21 992 HUMRETBLAS 21 1111 16 HUMRETBLAS 23 250 HUMRETBLAS 23 644 HUMRETBLAS 23 867 HUMRETBLAS 23 4625 HUMRETBLAS 23 5629 HUMRETBLAS 23 5748 HUMRETBLAS 23 5982 HUMRETBLAS 23 6107 HUMRETBLAS 23 6149 HUMRETBLAS 23 6290 HUMRETBLAS 23 6385 HUMRETBLAS 23 6432 HUMRETBLAS 23 6961 HUMRETBLAS 23 7155 HUMRETBLAS 23 7815 HUMRETBLAS 23 7891 17 HUMRETBLAS 24 38 HUMRETBLAS 24 275 HUMRETBLAS 24 666 HUMRETBLAS 24 1072 HUMRETBLAS 24 1076 HUMRETBLAS 24 1164 HUMRETBLAS 24 1759 HUMRETBLAS 24 2302 HUMRETBLAS 24 2316 HUMRETBLAS 24 2365 HUMRETBLAS 24 2379 HUMRETBLAS 24 2416 HUMRETBLAS 24 2841 HUMRETBLAS 24 3000 HUMRETBLAS 24 3059 HUMRETBLAS 24 3125 19 HUMRETBLAS 25 367 HUMRETBLAS 25 420 2 HUMRETBLAS 26 101 HUMRETBLAS 26 136 HUMRETBLAS 26 186 HUMRETBLAS 26 531 HUMRETBLAS 26 653 HUMRETBLAS 26 665 HUMRETBLAS 26 1591 HUMRETBLAS 26 1727 HUMRETBLAS 26 2122 24 HSHLADZA 2 377 66 HSHLADZA 4 59 HSHLADZA 4 134 HSHLADZA 4 139 HSHLADZA 4 164 197 HUMTBGA 1 222 HUMTBGA 1 289 HUMTBGA 1 294 HUMTBGA 1 527 HUMTBGA 1 533 HUMTBGA 1 571 HUMTBGA 1 937 30 HUMTBGA 2 30 HUMTBGA 2 48 HUMTBGA 2 361 HUMTBGA 2 575 HUMTBGA 2 694 2 HUMTBGA 3 165 HUMTBGA 3 241 HUMTBGA 3 250 HUMTBGA 3 272 HUMTBGA 3 296 HUMTBGA 3 332 7 HSAT3 1 8 HSAT3 1 178 HSAT3 1 1289 HSAT3 1 1578 HSAT3 1 1627 HSAT3 1 2199 2 HSAT3 2 1110 HSAT3 2 1511 HSAT3 2 1666 HSAT3 2 1783 HSAT3 2 1999 HSAT3 2 2435 148 HSAT3 3 585 HSAT3 3 751 HSAT3 3 819 HSAT3 3 874 22 HSAT3 4 128 HSAT3 4 141 175 HSAT3 5 232 HSAT3 5 532 HSAT3 5 741 HSAT3 5 1011 HSAT3 5 1142 HSAT3 5 1413 HSAT3 5 1785 HSAT3 5 1827 HSAT3 5 1901 48 HSAT3 6 546 HSAT3 6 901 HSAT3 6 918 HSAT3 6 1452 HSAT3 6 2153 HSAT3 6 2317 HSAT3 6 2432 HSAT3 6 2634 HSAT3 6 2654 HSAT3 6 2821 25 HUMCACY 1 78 109 HSUPA 1 302 19 HSUPA 3 90 HSUPA 3 95 HSUPA 3 169 HSUPA 3 174 HSUPA 3 314 HSUPA 3 545 93 HSUPA 4 4 2 HSUPA 5 27 HSUPA 5 86 12 HSUPA 7 526 33 HSUPA 8 94 HSUPA 8 171 HSUPA 8 201 6 HSUPA 9 249 HSUPA 9 266 HSUPA 9 309 HSUPA 9 355 HSUPA 9 398 HSUPA 9 704 HSUPA 9 785 73 HUMCNP 1 291 HSU29953 1 382 HSU29953 1 424 HSU29953 1 651 HSU29953 1 728 HSU29953 1 1110 HSU29953 1 1205 HSU29953 1 1221 HSU29953 1 1696 HSU29953 1 2051 HSU29953 1 2093 HSU29953 1 2125 HSU29953 1 2203 HSU29953 1 2434 190 HSU29953 2 310 HSU29953 2 328 72 HSU29953 3 331 270 HSU29953 4 1567 HSU29953 4 1887 HSU29953 4 2220 HSU29953 4 2401 HSU29953 4 2535 HSU29953 4 2663 HSU29953 4 2665 48 HSU29953 5 133 HSU29953 5 228 HSU29953 5 568 HSU29953 5 779 HSU29953 5 894 HSU29953 5 1118 79 HSU29953 6 26 126 HUMAFP 2 48 HUMAFP 2 371 HUMAFP 2 411 HUMAFP 2 594 HUMAFP 2 923 2 HUMAFP 3 170 HUMAFP 3 371 HUMAFP 3 472 HUMAFP 3 613 HUMAFP 3 722 HUMAFP 3 976 HUMAFP 3 1189 HUMAFP 3 1230 HUMAFP 3 1270 HUMAFP 3 1402 HUMAFP 3 1408 HUMAFP 3 1460 HUMAFP 3 1603 HUMAFP 3 1637 HUMAFP 3 1785 HUMAFP 3 1798 HUMAFP 3 2247 10 HUMAFP 4 18 HUMAFP 4 144 HUMAFP 4 168 HUMAFP 4 537 HUMAFP 4 983 HUMAFP 4 1079 HUMAFP 4 1448 2 HUMAFP 5 215 HUMAFP 5 291 HUMAFP 5 403 HUMAFP 5 694 HUMAFP 5 874 43 HUMAFP 6 28 HUMAFP 6 180 HUMAFP 6 602 2 HUMAFP 7 115 HUMAFP 7 579 HUMAFP 7 595 HUMAFP 7 975 HUMAFP 7 1280 HUMAFP 7 1360 HUMAFP 7 1368 HUMAFP 7 1397 HUMAFP 7 1700 HUMAFP 7 1860 HUMAFP 7 2075 19 HUMAFP 8 107 HUMAFP 8 644 HUMAFP 8 859 HUMAFP 8 943 HUMAFP 8 1161 HUMAFP 8 1309 2 HUMAFP 11 279 HUMAFP 11 1089 HUMAFP 11 1224 HUMAFP 11 1228 HUMAFP 11 1241 HUMAFP 11 1352 HUMAFP 11 1360 HUMAFP 11 1470 55 HUMAFP 12 614 HUMAFP 12 723 HUMAFP 12 1005 HUMAFP 12 1014 2 HUMAFP 13 258 HUMAFP 13 280 HUMAFP 13 865 HSRODPDE 1 98 HSRODPDE 1 276 HSRODPDE 1 499 HSRODPDE 1 638 HSRODPDE 1 670 HSRODPDE 1 795 HSRODPDE 1 1107 2 HSRODPDE 2 215 114 HUMINCP 1 252 HUMINCP 1 1045 HUMINCP 1 1213 HUMINCP 1 1459 97 HUMINCP 2 45 HUMINCP 2 85 HUMINCP 2 101 HUMINCP 2 105 HUMINCP 2 173 HUMINCP 2 195 HUMINCP 2 229 HUMINCP 2 315 HUMINCP 2 337 HUMINCP 2 355 HUMINCP 2 421 HUMINCP 2 920 HUMINCP 2 995 HUMINCP 2 999 10 AF005058 1 161 AF005058 1 199 AF005058 1 299 AF005058 1 496 AF005058 1 516 AF005058 1 767 AF005058 1 853 AF005058 1 1847 AF005058 1 2100 202 HUMIFNRF1A 1 108 HUMIFNRF1A 1 199 HUMIFNRF1A 1 546 HUMIFNRF1A 1 647 HUMIFNRF1A 1 1018 HUMIFNRF1A 1 1347 37 HUMIFNRF1A 2 211 HUMIFNRF1A 2 698 90 HUMIFNRF1A 3 54 HUMIFNRF1A 4 47 85 HUMIFNRF1A 5 34 HUMIFNRF1A 6 199 HUMIFNRF1A 6 280 HUMIFNRF1A 6 397 HUMIFNRF1A 6 482 159 HUMIFNRF1A 7 180 HUMIFNRF1A 7 239 HUMIFNRF1A 7 431 HUMIFNRF1A 7 498 HUMIFNRF1A 7 516 HUMIFNRF1A 7 1106 34 HUMGCAPB 1 69 HUMGCAPB 1 148 HUMGCAPB 1 717 HUMGCAPB 1 794 HUMGCAPB 1 805 HUMGCAPB 1 856 HUMGCAPB 1 1186 HUMGCAPB 1 1269 58 HUMGCAPB 3 68 HUMGCAPB 3 84 75 S73906 1 78 2 S73906 2 41 2 HSB3A 1 3 HSB3A 1 96 HSB3A 1 241 HSB3A 1 779 HSB3A 1 811 HSB3A 1 826 2 HSCYCLA 1 28 HSCYCLA 1 136 58 HSCYCLA 2 32 HSCYCLA 2 102 HSCYCLA 2 139 HSCYCLA 2 375 HSCYCLA 2 547 HSCYCLA 2 624 9 HSCYCLA 4 351 HSCYCLA 4 369 2 HSCYCLA 5 26 HSCYCLA 5 50 HSCYCLA 5 389 7 HSCYCLA 6 158 HSCYCLA 6 248 HSCYCLA 6 411 HSCYCLA 6 571 37 HSCYCLA 7 198 HSCYCLA 7 314 2 HUMHCF2 1 54 HUMHCF2 1 352 HUMHCF2 1 440 HUMHCF2 1 873 HUMHCF2 1 1183 HUMHCF2 1 1559 HUMHCF2 1 2072 HUMHCF2 1 2641 HUMHCF2 1 3205 HUMHCF2 1 3509 HUMHCF2 1 3710 66 HUMHCF2 2 618 HUMHCF2 2 700 HUMHCF2 2 1160 HUMHCF2 2 1171 HUMHCF2 2 1303 161 HUMHCF2 3 233 154 AC004130 1 89 AC004130 1 808 AC004130 1 846 AC004130 1 1195 AC004130 1 1888 AC004130 1 2516 AC004130 1 3881 AC004130 1 4602 AC004130 1 4628 AC004130 1 5040 AC004130 1 5646 AC004130 1 5787 AC004130 1 6004 AC004130 1 6037 AC004130 1 6078 AC004130 1 6118 AC004130 1 6197 AC004130 1 6230 AC004130 1 6461 AC004130 1 7028 AC004130 1 7044 AC004130 1 7363 AC004130 1 7434 AC004130 1 7469 AC004130 1 7473 AC004130 1 7862 AC004130 1 8377 AC004130 1 8534 AC004130 1 8538 AC004130 1 8740 AC004130 1 8819 AC004130 1 9501 AC004130 1 9940 AC004130 1 10090 AC004130 1 10246 AC004130 1 10310 AC004130 1 10536 AC004130 1 11002 AC004130 1 11032 AC004130 1 11464 AC004130 1 11636 AC004130 1 11828 AC004130 1 11950 AC004130 1 11974 AC004130 1 12145 AC004130 1 13149 AC004130 1 13356 AC004130 1 13504 AC004130 1 13576 AC004130 1 13688 AC004130 1 13845 AC004130 1 13964 AC004130 1 14076 AC004130 1 14082 AC004130 1 14112 AC004130 1 14126 AC004130 1 14189 AC004130 1 14282 AC004130 1 14561 AC004130 1 14587 AC004130 1 14704 AC004130 1 14794 AC004130 1 14932 AC004130 1 15027 AC004130 1 15071 AC004130 1 15276 AC004130 1 15423 AC004130 1 15430 AC004130 1 15443 AC004130 1 15590 AC004130 1 15676 AC004130 1 15807 AC004130 1 15856 AC004130 1 16032 AC004130 1 16214 AC004130 1 16337 AC004130 1 16699 AC004130 1 16708 AC004130 1 16733 AC004130 1 17257 AC004130 1 17399 AC004130 1 17411 AC004130 1 17682 AC004130 1 17973 AC004130 1 18127 AC004130 1 18449 AC004130 1 18629 AC004130 1 19443 AC004130 1 19531 AC004130 1 19695 AC004130 1 19837 AC004130 1 20380 AC004130 1 21567 AC004130 1 21571 AC004130 1 21784 AC004130 1 22419 AC004130 1 22535 AC004130 1 22563 AC004130 1 22906 AC004130 1 23300 AC004130 1 23524 AC004130 1 24337 AC004130 1 24442 AC004130 1 25052 AC004130 1 25569 AC004130 1 25775 AC004130 1 25787 AC004130 1 26174 AC004130 1 26306 AC004130 1 26496 AC004130 1 26704 AC004130 1 26819 AC004130 1 27422 AC004130 1 27698 AC004130 1 27710 AC004130 1 28103 AC004130 1 28171 AC004130 1 28540 AC004130 1 28645 AC004130 1 28767 AC004130 1 28885 AC004130 1 29390 AC004130 1 29440 AC004130 1 29790 AC004130 1 30250 AC004130 1 30526 AC004130 1 30953 AC004130 1 31020 AC004130 1 31256 AC004130 1 31506 159 AC004130 2 83 AC004130 2 206 AC004130 2 850 AC004130 2 1505 AC004130 2 2097 AC004130 2 2105 AC004130 2 2197 AC004130 2 2371 AC004130 2 2760 AC004130 2 2828 AC004130 2 2908 AC004130 2 3239 34 AC004130 3 251 AC004130 3 348 AC004130 3 359 AC004130 3 1064 AC004130 3 1076 AC004130 3 1639 AC004130 3 1812 AC004130 3 1887 AC004130 3 2022 AC004130 3 2094 AC004130 3 2192 AC004130 3 2409 AC004130 3 3524 AC004130 3 3662 AC004130 3 3779 AC004130 3 3928 AC004130 3 4475 AC004130 3 4489 AC004130 3 5022 AC004130 3 5191 AC004130 3 5234 AC004130 3 5435 AC004130 3 5501 AC004130 3 5583 AC004130 3 5587 AC004130 3 6002 AC004130 3 6789 AC004130 3 7131 AC004130 3 7205 AC004130 3 7254 AC004130 3 7457 AC004130 3 7597 AC004130 3 7681 AC004130 3 7880 AC004130 3 7889 AC004130 3 8105 AC004130 3 8148 AC004130 3 8158 AC004130 3 8392 AC004130 3 8749 AC004130 3 8850 AC004130 3 9305 AC004130 3 10658 AC004130 3 10768 AC004130 3 11106 AC004130 3 11787 18 AC004130 4 125 AC004130 4 130 AC004130 4 266 AC004130 4 464 AC004130 4 499 AC004130 4 833 32 AC004130 5 140 AC004130 5 153 AC004130 5 832 16 AC004130 6 284 AC004130 6 544 AC004130 6 907 AC004130 6 911 AC004130 6 1247 AC004130 6 1399 AC004130 6 2130 AC004130 6 2523 AC004130 6 2699 AC004130 6 3332 AC004130 6 3384 AC004130 6 4036 AC004130 6 4153 AC004130 6 4213 AC004130 6 4964 AC004130 6 5118 AC004130 6 5469 AC004130 6 6663 AC004130 6 6804 AC004130 6 6871 AC004130 6 7564 AC004130 6 7653 AC004130 6 7730 AC004130 6 8940 AC004130 6 9167 AC004130 6 9414 AC004130 6 9426 13 AC004130 7 42 AC004130 7 186 AC004130 7 450 AC004130 7 553 AC004130 7 1039 AC004130 7 1150 AC004130 7 1254 AC004130 7 1354 AC004130 7 2730 7 AC004130 8 365 AC004130 8 754 AC004130 8 757 AC004130 8 889 AC004130 8 1225 AC004130 8 1237 AC004130 8 1551 AC004130 8 1865 AC004130 8 2341 AC004130 8 2475 AC004130 8 3069 AC004130 8 3174 AC004130 8 3847 13 AC004130 9 3 AC004130 9 215 AC004130 9 381 AC004130 9 520 AC004130 9 724 AC004130 9 1627 AC004130 9 1632 AC004130 9 2126 AC004130 9 2261 AC004130 9 2688 37 AC004130 10 166 AC004130 10 358 AC004130 10 701 AC004130 10 1349 AC004130 10 1680 AC004130 10 1961 AC004130 10 2101 AC004130 10 2189 AC004130 10 2455 90 AC004130 11 326 AC004130 11 858 AC004130 11 998 AC004130 11 1022 164 AC004130 12 165 AC004130 12 455 AC004130 12 998 AC004130 12 1245 AC004130 12 1250 AC004130 12 1921 AC004130 12 2025 AC004130 12 2476 AC004130 12 2502 AC004130 12 2786 AC004130 12 3189 AC004130 12 3300 42 HSIFNG 1 386 HSIFNG 1 457 HSIFNG 1 474 HSIFNG 1 592 16 HSIFNG 3 154 HSIFNG 3 188 HSIFNG 3 237 HSIFNG 3 266 HSIFNG 3 270 HSIFNG 3 401 HSIFNG 3 1037 HSIFNG 3 1455 HSIFNG 3 1514 HSIFNG 3 1820 HSIFNG 3 2102 HSIFNG 3 2253 HSIFNG 3 2287 HSIFNG 3 2306 121 HUMNUCLEO 1 172 HUMNUCLEO 1 445 HUMNUCLEO 1 691 HUMNUCLEO 1 827 31 HUMNUCLEO 2 98 HUMNUCLEO 2 177 HUMNUCLEO 2 848 HUMNUCLEO 2 937 61 HUMNUCLEO 3 41 HUMNUCLEO 3 232 HUMNUCLEO 3 473 HUMNUCLEO 3 517 HUMNUCLEO 3 653 18 HUMNUCLEO 6 112 HUMNUCLEO 6 346 HUMNUCLEO 6 506 HUMNUCLEO 6 531 HUMNUCLEO 6 806 2 HUMNUCLEO 7 3 HUMNUCLEO 7 163 HUMNUCLEO 7 191 HUMNUCLEO 7 521 6 HUMNUCLEO 8 19 HUMNUCLEO 8 111 HUMNUCLEO 8 165 HUMNUCLEO 8 234 HUMNUCLEO 8 261 HUMNUCLEO 8 308 HUMNUCLEO 8 398 59 HUMNUCLEO 9 106 HUMNUCLEO 9 110 HUMNUCLEO 9 267 HUMNUCLEO 9 319 HUMNUCLEO 9 356 54 HUMNUCLEO 10 60 HUMNUCLEO 10 200 2 HUMNUCLEO 12 14 HUMNUCLEO 12 180 HUMNUCLEO 12 347 2 HSP53G 3 486 HSP53G 3 655 100 HSP53G 5 62 HSP53G 5 129 37 HSP53G 6 288 227 HSP53G 8 309 HSP53G 8 332 HSP53G 8 1235 HSP53G 8 1408 HSP53G 8 1534 HSP53G 8 1829 HSP53G 8 1856 HSP53G 8 2008 HSP53G 8 2091 HSP53G 8 2418 HSP53G 8 2682 115 HSP53G 9 364 HSP53G 9 405 HSP53G 9 633 HSP53G 9 718 2 AF039307 1 311 AF039307 1 364 AF039307 1 1030 51 HSMYBPC3 1 187 HSMYBPC3 1 193 HSMYBPC3 1 204 HSMYBPC3 1 865 HSMYBPC3 1 1006 81 HSMYBPC3 2 83 HSMYBPC3 2 433 HSMYBPC3 2 577 24 HSMYBPC3 3 81 HSMYBPC3 3 127 HSMYBPC3 3 143 39 HSMYBPC3 5 47 HSMYBPC3 5 420 HSMYBPC3 5 529 HSMYBPC3 5 1040 100 HSMYBPC3 6 292 HSMYBPC3 6 373 105 HSMYBPC3 7 106 HSMYBPC3 7 146 2 HSMYBPC3 9 32 2 HSMYBPC3 10 41 HSMYBPC3 10 84 HSMYBPC3 10 125 2 HSMYBPC3 12 73 HSMYBPC3 12 110 HSMYBPC3 12 232 HSMYBPC3 12 789 HSMYBPC3 12 1206 HSMYBPC3 12 1298 3 HSMYBPC3 13 34 86 HSMYBPC3 17 167 HSMYBPC3 17 208 24 HSMYBPC3 18 16 HSMYBPC3 18 654 HSMYBPC3 18 701 2 HSMYBPC3 19 20 18 HSMYBPC3 20 236 HSMYBPC3 20 750 HSMYBPC3 20 780 HSMYBPC3 20 806 HSMYBPC3 20 826 HSMYBPC3 20 840 HSMYBPC3 20 897 HSMYBPC3 20 947 18 HSMYBPC3 21 40 HSMYBPC3 21 146 34 HSMYBPC3 22 14 HSMYBPC3 22 104 HSMYBPC3 22 428 307 HSMYBPC3 23 297 HSMYBPC3 23 435 HSMYBPC3 23 636 HSMYBPC3 23 699 300 HSMYBPC3 24 24 HSMYBPC3 25 728 HSMYBPC3 25 984 45 HSMYBPC3 26 300 HSMYBPC3 26 472 75 HSMYBPC3 27 66 HSMYBPC3 27 247 HSMYBPC3 27 319 HSMYBPC3 27 500 HSMYBPC3 27 581 HSMYBPC3 27 831 219 HSMHCPU15 1 81 HSMHCPU15 1 852 HSMHCPU15 1 1382 196 HSMHCPU15 2 148 HSMHCPU15 2 427 HSMHCPU15 2 763 HSMHCPU15 2 780 HSMHCPU15 2 860 HSMHCPU15 2 1029 2 HSMHCPU15 3 272 HSMHCPU15 3 397 20 HSMHCPU15 5 495 HSMHCPU15 5 523 HSMHCPU15 5 797 63 HUMMHCD8A 2 503 246 HUMMHCD8A 4 239 HUMMHCD8A 4 343 HUMMHCD8A 4 370 60 HUMMHCD8A 5 572 HUMMHCD8A 5 1250 HUMMHCD8A 5 2154 HUMMHCD8A 5 2208 HUMMHCD8A 5 2405 2 HUMPALC 1 58 HUMPALC 1 225 HUMPALC 1 528 34 HUMPALC 2 288 HUMPALC 2 292 HUMPALC 2 360 HUMPALC 2 1623 HUMPALC 2 2005 2 HUMPALC 3 105 HUMPALC 3 418 HUMPALC 3 574 HUMPALC 3 821 HUMPALC 3 1521 HUMPALC 3 1632 HUMPALC 3 1931 HUMPALC 3 2023 HUMPALC 3 2065 HUMPALC 3 2154 HUMPALC 3 2246 HUMPALC 3 3239 HUMPALC 3 3248 115 HSRA36 2 415 HSRA36 2 833 HSRA36 2 878 HSRA36 2 894 HSRA36 2 1166 HSRA36 2 1434 HSRA36 2 1519 HSRA36 2 1548 HSRA36 2 2639 HSRA36 2 2915 HSRA36 2 3060 HSRA36 2 3108 HSRA36 2 3298 7 HSRA36 3 82 HSRA36 3 270 HSRA36 3 702 HSRA36 3 930 HSRA36 3 963 HSRA36 3 1208 HSRA36 3 1235 HSRA36 3 1435 HSRA36 3 1476 HSRA36 3 1641 HSRA36 3 1937 HSRA36 3 1985 186 HSFOLA 1 154 HSFOLA 1 181 HSFOLA 1 285 HSFOLA 1 289 HSFOLA 1 316 HSFOLA 1 421 HSFOLA 1 734 HSFOLA 1 768 HSFOLA 1 875 HSFOLA 1 888 HSFOLA 1 1071 HSFOLA 1 1210 HSFOLA 1 1807 HSFOLA 1 1833 139 HSFOLA 3 5 HSFOLA 3 40 12 HUMIL9RA 1 344 HUMIL9RA 1 514 HUMIL9RA 1 926 HUMIL9RA 1 1103 HUMIL9RA 1 1463 HUMIL9RA 1 1596 HUMIL9RA 1 1663 HUMIL9RA 1 2110 HUMIL9RA 1 2201 HUMIL9RA 1 2409 HUMIL9RA 1 2521 HUMIL9RA 1 2538 HUMIL9RA 1 2857 HUMIL9RA 1 2895 HUMIL9RA 1 3205 HUMIL9RA 1 3450 HUMIL9RA 1 3550 HUMIL9RA 1 3720 HUMIL9RA 1 4129 HUMIL9RA 1 4327 HUMIL9RA 1 4341 HUMIL9RA 1 4983 HUMIL9RA 1 5009 HUMIL9RA 1 5019 42 HUMIL9RA 2 29 HUMIL9RA 2 259 HUMIL9RA 2 324 27 HUMIL9RA 3 39 2 HUMIL9RA 4 85 HUMIL9RA 4 97 HUMIL9RA 4 438 15 HUMIL9RA 5 122 HUMIL9RA 5 169 HUMIL9RA 5 188 HUMIL9RA 5 227 HUMIL9RA 5 239 HUMIL9RA 5 263 HUMIL9RA 5 311 HUMIL9RA 5 325 HUMIL9RA 5 350 HUMIL9RA 5 392 HUMIL9RA 5 401 HUMIL9RA 5 531 HUMIL9RA 5 537 HUMIL9RA 5 568 HUMIL9RA 5 577 HUMIL9RA 5 603 HUMIL9RA 5 641 58 HUMIL9RA 6 151 HUMIL9RA 6 421 HUMIL9RA 6 463 HUMIL9RA 6 537 141 HUMIL9RA 7 3 HUMIL9RA 7 54 HUMIL9RA 7 92 HUMIL9RA 7 103 HUMIL9RA 7 525 HUMIL9RA 7 808 HUMIL9RA 7 842 HUMIL9RA 7 873 HUMIL9RA 7 914 HUMIL9RA 7 933 HUMIL9RA 7 1233 2 HUMIL9RA 8 247 HUMIL9RA 8 332 HUMIL9RA 8 366 HUMIL9RA 8 617 HUMIL9RA 8 900 HUMIL9RA 8 943 HUMIL9RA 8 1040 HUMIL9RA 8 1060 HUMIL9RA 8 1352 HUMIL9RA 8 1548 HUMIL9RA 8 1680 79 HUMRCP 1 722 HUMRCP 1 780 HUMRCP 1 1034 HUMRCP 1 1340 HUMRCP 1 1381 HUMRCP 1 1474 HUMRCP 1 1562 HUMRCP 1 1603 HUMRCP 1 1811 HUMRCP 1 2160 HUMRCP 1 2295 HUMRCP 1 2302 HUMRCP 1 2322 HUMRCP 1 2878 HUMRCP 1 3193 HUMRCP 1 3322 HUMRCP 1 3352 HUMRCP 1 3411 HUMRCP 1 3848 HUMRCP 1 3870 HUMRCP 1 4658 HUMRCP 1 5225 HUMRCP 1 5555 HUMRCP 1 5797 HUMRCP 1 5839 HUMRCP 1 6056 HUMRCP 1 6162 HUMRCP 1 6723 HUMRCP 1 6804 HUMRCP 1 7143 HUMRCP 1 7428 HUMRCP 1 7499 HUMRCP 1 7605 HUMRCP 1 7947 HUMRCP 1 8782 HUMRCP 1 8858 HUMRCP 1 8967 HUMRCP 1 8971 HUMRCP 1 9491 HUMRCP 1 9688 HUMRCP 1 10042 HUMRCP 1 10103 HUMRCP 1 10233 HUMRCP 1 11203 HUMRCP 1 11776 HUMRCP 1 12158 HUMRCP 1 12235 262 HUMRCP 2 8 HUMRCP 2 304 HUMRCP 2 406 HUMRCP 2 493 HUMRCP 2 962 HUMRCP 2 1063 HUMRCP 2 1135 HUMRCP 2 1982 HUMRCP 2 1999 HUMRCP 2 2198 HUMRCP 2 2534 111 HUMRCP 3 93 HUMRCP 3 197 HUMRCP 3 268 HUMRCP 3 313 HUMRCP 3 630 HUMRCP 3 752 HUMRCP 3 1766 HUMRCP 3 1802 HUMRCP 3 1970 172 HUMRCP 4 340 HUMRCP 4 593 HUMRCP 4 711 HUMRCP 4 1465 HUMRCP 4 2022 HUMRCP 4 2097 HUMRCP 4 2137 HUMRCP 4 2227 HUMRCP 4 2408 HUMRCP 4 2489 HUMRCP 4 2840 30 HSN44A4 1 414 HSN44A4 1 667 HSN44A4 1 678 HSN44A4 1 1005 HSN44A4 1 1253 HSN44A4 1 1262 HSN44A4 1 1313 HSN44A4 1 1397 HSN44A4 1 1455 HSN44A4 1 1697 HSN44A4 1 1813 HSN44A4 1 2168 HSN44A4 1 2331 HSN44A4 1 2390 HSN44A4 1 2534 HSN44A4 1 2665 HSN44A4 1 2975 HSN44A4 1 2993 HSN44A4 1 3111 HSN44A4 1 3515 HSN44A4 1 3556 HSN44A4 1 4017 HSN44A4 1 4073 HSN44A4 1 4272 HSN44A4 1 4933 HSN44A4 1 5064 HSN44A4 1 5602 HSN44A4 1 5908 HSN44A4 1 6351 HSN44A4 1 6530 HSN44A4 1 6534 HSN44A4 1 6789 HSN44A4 1 6824 HSN44A4 1 6852 HSN44A4 1 6872 HSN44A4 1 6930 HSN44A4 1 6983 HSN44A4 1 7091 HSN44A4 1 7360 HSN44A4 1 7801 HSN44A4 1 7998 HSN44A4 1 8629 HSN44A4 1 8746 HSN44A4 1 8750 HSN44A4 1 8869 HSN44A4 1 8892 HSN44A4 1 8994 HSN44A4 1 9301 HSN44A4 1 9769 HSN44A4 1 10278 HSN44A4 1 10282 HSN44A4 1 11035 277 HUMDODDA 2 43 HUMDODDA 2 610 HUMDODDA 2 683 HUMDODDA 2 767 HUMDODDA 2 1194 HUMDODDA 2 1336 HUMDODDA 2 1505 HUMDODDA 2 1663 HUMDODDA 2 1776 HUMDODDA 2 1792 HUMDODDA 2 2064 HUMDODDA 2 2325 HUMDODDA 2 2693 HUMDODDA 2 2871 HUMDODDA 2 2897 HUMDODDA 2 2909 HUMDODDA 2 3137 HUMDODDA 2 3158 HUMDODDA 2 3270 HUMDODDA 2 3274 HUMDODDA 2 3323 HUMDODDA 2 3621 HUMDODDA 2 3637 HUMDODDA 2 3973 HUMDODDA 2 4156 HUMDODDA 2 4246 HUMDODDA 2 4392 HUMDODDA 2 4506 HUMDODDA 2 4520 HUMDODDA 2 4716 HUMDODDA 2 5193 HUMDODDA 2 5660 HUMDODDA 2 5948 HUMDODDA 2 6070 HUMDODDA 2 6457 HUMDODDA 2 7019 HUMDODDA 2 7092 HUMDODDA 2 7538 HUMDODDA 2 7671 HUMDODDA 2 8209 HUMDODDA 2 8255 HUMDODDA 2 8841 HUMDODDA 2 8876 HUMDODDA 2 8965 HUMDODDA 2 9116 HUMDODDA 2 9164 HUMDODDA 2 9168 HUMDODDA 2 9262 HUMDODDA 2 9670 HUMDODDA 2 9677 HUMDODDA 2 9770 HUMDODDA 2 10083 HUMDODDA 2 10776 HUMDODDA 2 10915 HUMDODDA 2 10990 HUMDODDA 2 11076 HUMDODDA 2 11287 HUMDODDA 2 12601 HUMDODDA 2 12898 HUMDODDA 2 12902 HUMDODDA 2 13364 HUMDODDA 2 13454 HUMDODDA 2 13818 HUMDODDA 2 14002 HUMDODDA 2 14414 HUMDODDA 2 14424 HUMDODDA 2 14489 HUMDODDA 2 14977 HUMDODDA 2 15070 HUMDODDA 2 15201 HUMDODDA 2 15266 HUMDODDA 2 15280 HUMDODDA 2 15687 HUMDODDA 2 16753 HUMDODDA 2 16794 HUMDODDA 2 16858 HUMDODDA 2 17030 HUMDODDA 2 17146 HUMDODDA 2 17378 HUMDODDA 2 17765 HUMDODDA 2 18167 HUMDODDA 2 18424 HUMDODDA 2 18626 HUMDODDA 2 18733 HUMDODDA 2 18880 HUMDODDA 2 19272 HUMDODDA 2 19364 HUMDODDA 2 20096 30 HUMDODDA 3 348 HUMDODDA 3 750 HUMDODDA 3 1254 HUMDODDA 3 1318 54 HUMDODDA 4 105 HUMDODDA 4 234 HUMDODDA 4 308 HUMDODDA 4 623 HUMDODDA 4 740 HUMDODDA 4 847 HUMDODDA 4 1100 HUMDODDA 4 1443 2 HSU79415 1 274 HSU79415 1 526 HSU79415 1 621 HSU79415 1 804 HSU79415 1 1046 HSU79415 1 1149 HSU79415 1 1271 HSU79415 1 1323 HSU79415 1 1327 HSU79415 1 1624 87 HSU53874 1 173 HSU53874 2 48 2 HSU53874 3 306 HSU53874 3 376 13 HSU53874 4 148 100 HSUBA52G 2 187 HSUBA52G 2 400 HSUBA52G 2 484 HSUBA52G 2 918 48 HSGGL2 2 507 HSGGL2 2 519 HSGGL2 2 785 136 HUMFABP 2 329 HUMFABP 2 385 HUMFABP 2 421 HUMFABP 2 572 HUMFABP 2 629 HUMFABP 2 828 HUMFABP 2 921 88 HUMPROT2 1 127 36 HSU20982 1 119 HSU20982 1 291 HSU20982 1 320 HSU20982 1 386 HSU20982 1 470 102 HSU20982 2 136 HSU20982 2 253 139 AF017178 1 205 AF017178 1 223 AF017178 1 294 AF017178 1 691 AF017178 1 907 AF017178 1 931 AF017178 1 1404 90 AF017178 4 34 AF017178 5 252 AF017178 5 642 286 AF017178 7 95 AF017178 9 185 145 AF017178 11 94 AF017178 11 176 AF017178 11 265 13 AF017178 25 10 AF017178 25 228 13 AF017178 28 31 34 AF017178 29 103 AF017178 29 181 AF017178 29 407 73 AF017178 30 31 91 AF017178 31 161 82 AF017178 32 209 25 AF017178 37 57 79 AF017178 39 33 AF017178 45 157 121 HSU32576 1 9 HSU32576 1 39 HSU32576 1 45 HSU32576 1 82 HSU32576 1 130 HSU32576 1 219 HSU32576 1 311 HSU32576 1 315 HSU32576 1 356 HSU32576 1 370 HSU32576 1 950 HSU32576 1 1154 HSU32576 1 1394 HSU32576 1 1470 HSU32576 1 1717 HSU32576 1 1882 HSU32576 1 1948 HSU32576 1 1966 48 HSU70732 1 96 HSU70732 4 65 31 HSU70732 5 83 HSU70732 5 125 HSU70732 5 167 HSU70732 5 209 HSU70732 8 26 34 HSU70732 9 24 31 HUMAK1 1 679 HUMAK1 1 773 HUMAK1 1 1212 HUMAK1 1 1484 48 HUMAK1 3 18 313 HUMAK1 4 90 HUMAK1 4 128 HUMAK1 4 1388 HUMAK1 4 1942 HUMAK1 4 1998 HUMAK1 4 2048 HUMAK1 4 2069 HUMAK1 4 2283 HUMAK1 4 2299 HUMAK1 4 2317 HUMAK1 4 2548 HUMAK1 4 2911 HUMAK1 4 2948 10 HUMAK1 5 184 HUMAK1 5 208 187 HSHOX3D 1 266 9 HSU40391 2 50 HSU40391 2 219 115 HSU07807 1 282 HSU07807 1 880 HSU07807 1 1225 HSU07807 1 1233 HSU07807 1 1723 HSU07807 1 1810 HSU07807 1 1894 HSU07807 1 1978 HSU07807 1 2071 HSU07807 1 2115 6 HSU07807 2 8 HSU07807 2 122 HSU07807 2 963 120 AF032455 1 3 AF032455 1 417 AF032455 1 708 AF032455 1 1248 AF032455 1 1443 AF032455 1 1454 AF032455 1 1498 AF032455 1 1502 AF032455 1 1681 AF032455 1 1826 AF032455 1 1985 AF032455 1 2064 AF032455 1 2315 AF032455 1 2384 AF032455 1 2422 AF032455 1 2569 AF032455 1 2819 AF032455 1 3029 AF032455 1 3187 AF032455 1 3267 AF032455 1 3540 AF032455 1 3552 AF032455 1 3851 AF032455 1 3900 AF032455 1 3934 AF032455 1 3963 AF032455 1 4068 AF032455 1 4510 AF032455 1 5206 AF032455 1 5459 AF032455 1 5514 AF032455 1 5932 AF032455 1 6487 AF032455 1 6526 79 AF032455 3 94 AF032455 3 435 AF032455 3 636 AF032455 3 701 AF032455 3 929 79 AF032455 4 367 238 AF032455 6 274 2 AF032455 7 75 AF032455 7 218 AF032455 7 270 49 AF032455 8 463 AF032455 8 583 AF032455 8 865 AF032455 8 1017 AF032455 8 1406 112 AF032455 9 143 AF032455 9 240 AF032455 9 300 AF032455 9 310 AF032455 9 433 AF032455 9 599 AF032455 9 608 AF032455 9 1296 AF032455 9 1412 AF032455 9 1594 AF032455 9 2294 2 HSU22027 2 17 87 HSU22027 3 89 195 HSU22027 4 298 199 HSU22027 5 179 HSU22027 5 193 HSU22027 5 382 HSU22027 5 386 HSU22027 5 499 HSU22027 5 575 HSU22027 5 584 76 HSU22027 6 101 HSU22027 6 196 141 HSU22027 8 139 HSU22027 8 520 81 HUMSOMI 1 74 HUMSOMI 1 219 HUMSOMI 1 568 HUMSOMI 1 689 97 HUMMKXX 3 182 HUMMKXX 3 422 HUMMKXX 3 443 87 AC002366 1 23 AC002366 1 160 AC002366 1 462 AC002366 1 548 AC002366 1 660 AC002366 1 985 AC002366 1 1536 22 AC002366 2 326 AC002366 2 337 AC002366 2 403 AC002366 2 685 AC002366 2 812 AC002366 2 857 AC002366 2 1148 AC002366 2 1197 AC002366 2 1317 AC002366 2 1343 AC002366 2 1366 40 AC002366 4 185 AC002366 4 209 AC002366 4 630 AC002366 4 799 AC002366 4 1234 13 HSCYTOK20 1 70 HSCYTOK20 1 417 HSCYTOK20 1 471 HSCYTOK20 1 1542 HSCYTOK20 1 1853 73 HSCYTOK20 2 133 HSCYTOK20 2 203 HSCYTOK20 2 315 HSCYTOK20 2 384 HSCYTOK20 2 396 HSCYTOK20 2 450 HSCYTOK20 2 936 HSCYTOK20 2 1209 HSCYTOK20 2 1351 HSCYTOK20 2 1646 2 HSCYTOK20 3 171 163 HSCYTOK20 4 20 16 HSCYTOK20 5 331 HSCYTOK20 5 556 HSCYTOK20 5 780 HSCYTOK20 5 859 13 HSCYTOK20 6 517 2 HSCYTOK20 7 77 HSCYTOK20 7 594 9 AF005260 1 214 AF005260 1 358 AF005260 1 449 AF005260 1 969 168 HSU50136 1 85 HSU50136 1 342 HSU50136 1 840 HSU50136 1 968 HSU50136 1 972 HSU50136 1 1285 18 HSV698D2 1 597 HSV698D2 1 1054 HSV698D2 1 1146 HSV698D2 1 1411 HSV698D2 1 1715 HSV698D2 1 2138 HSV698D2 1 2354 HSV698D2 1 2358 HSV698D2 1 2751 HSV698D2 1 2948 HSV698D2 1 2990 HSV698D2 1 2994 HSV698D2 1 3270 HSV698D2 1 3910 HSV698D2 1 3923 HSV698D2 1 3941 HSV698D2 1 3975 HSV698D2 1 4307 HSV698D2 1 4359 HSV698D2 1 4518 HSV698D2 1 4739 HSV698D2 1 4837 HSV698D2 1 5434 HSV698D2 1 5504 HSV698D2 1 5697 HSV698D2 1 6198 HSV698D2 1 6232 HSV698D2 1 6521 HSV698D2 1 6646 HSV698D2 1 6749 HSV698D2 1 6796 HSV698D2 1 7279 HSV698D2 1 7890 HSV698D2 1 8055 HSV698D2 1 8405 18 HSV698D2 2 256 HSV698D2 2 298 HSV698D2 2 400 HSV698D2 2 463 HSV698D2 2 472 HSV698D2 2 540 HSV698D2 2 564 2 HSV698D2 3 145 HSV698D2 3 355 HSV698D2 3 424 28 HSV698D2 4 84 75 HSV698D2 5 168 HSV698D2 5 253 HSV698D2 5 404 HSV698D2 5 481 82 HSV698D2 6 27 HSV698D2 6 222 HSV698D2 6 598 HSV698D2 6 693 HSV698D2 6 872 7 HUMALIFA 1 508 HUMALIFA 1 909 HUMALIFA 1 1066 HUMALIFA 1 1277 HUMALIFA 1 1320 HUMALIFA 1 1609 507 HUMALIFA 2 224 HUMALIFA 2 369 49 HSU80184 1 783 HSU80184 1 787 HSU80184 1 1083 HSU80184 1 1177 HSU80184 1 1287 HSU80184 1 1503 HSU80184 1 1564 286 HSU80184 2 46 HSU80184 2 150 HSU80184 2 169 40 HSU80184 3 218 HSU80184 3 620 HSU80184 3 758 HSU80184 3 840 HSU80184 3 1142 HSU80184 3 1170 61 HSU80184 4 140 34 HSU80184 5 28 HSU80184 5 61 HSU80184 6 299 41 HSU80184 7 197 156 HSU80184 9 399 59 HSU80184 10 123 HSU80184 10 192 HSU80184 10 266 HSU80184 10 279 85 HSU80184 11 96 54 HSU80184 12 128 67 HSU80184 13 95 HSU80184 13 102 214 HSU80184 14 79 HSU80184 14 92 HSU80184 14 165 HSU80184 14 391 HSU80184 14 632 HSU80184 14 677 HSU80184 14 936 HSU80184 14 1265 13 HSU80184 15 5 2 HSU80184 16 14 HSU80184 16 19 HSU80184 16 64 2 HSU80184 18 462 145 HSU80184 20 274 HSU80184 23 67 HSU80184 23 87 112 HSU80184 29 25 HSRPII145 4 25 HSRPII145 4 30 2 HSRPII145 5 68 HSRPII145 5 144 22 HSU23143 1 270 64 HSU23143 3 187 2 HSU23143 5 42 HSU23143 5 50 HSU23143 6 230 122 HSU23143 8 11 HSU23143 8 18 21 HSU51243 1 172 HSU51243 1 550 HSU51243 1 1609 HSU51243 1 1851 HSU51243 1 1865 33 HSU51243 2 73 2 HSU51243 3 3 HSU51243 3 569 HSU51243 3 713 HSU51243 3 879 HSU51243 3 1406 262 HSU51243 4 231 HSU51243 4 249 HSU51243 4 419 2 HSU51243 5 254 HSU51243 5 271 HSU51243 5 458 HSU51243 5 482 22 HSU51243 6 115 HSU51243 6 183 HSU51243 6 231 HSU51243 6 450 2 H5U51243 7 107 HSU51243 7 619 HSU51243 7 741 HSU51243 7 915 HSU51243 7 1125 HSU51243 7 1254 HSU51243 7 1801 HSU51243 7 1875 HSU51243 7 2039 HSU51243 7 2098 HSU51243 7 2310 HSU51243 7 2453 HSU51243 7 2812 HSU51243 7 2866 HSU51243 7 2951 HSU51243 7 3004 13 HSU51243 8 341 HSU51243 8 845 HSU51243 8 916 HSU51243 8 944 HSU51243 8 1065 HSU51243 8 1099 HSU51243 8 1106 HSU51243 8 1110 HSU51243 8 1251 HSU51243 8 1519 HSU51243 8 1578 HSU51243 8 1973 HSU51243 8 2347 HSU51243 8 2457 2 HSU51243 9 99 HSU51243 9 1197 HSU51243 9 1833 HSU51243 9 1988 115 HSU51243 10 323 HSU51243 10 680 HSU51243 10 807 HSU51243 10 1038 164 HSU51243 11 317 79 HSU51243 12 1109 HSU51243 12 1474 8 HSU51243 13 228 HSU51243 13 508 HSU51243 13 756 HSU51243 13 900 22 AF015812 1 33 AF015812 1 363 AF015812 1 376 AF015812 1 380 AF015812 1 964 AF015812 1 993 AF015812 1 1240 11 AF015812 2 69 AF015812 2 130 AF015812 2 154 AF015812 2 228 97 AF015812 4 52 AF015812 4 77 25 AF015812 5 93 AF015812 5 194 46 AF015812 8 68 AF015812 8 82 AF015812 8 286 2 AF015812 9 177 8 AF015812 11 214 AF015812 11 418 AF015812 11 534 AF015812 11 587 AF015812 11 679 AF015812 11 750 3 AF015812 12 73 12 D87675 1 1051 D87675 1 1345 D87675 1 1680 D87675 1 1968 D87675 1 2126 D87675 1 2169 D87675 1 2173 D87675 1 2237 D87675 1 2290 D87675 1 2384 D87675 1 2398 D87675 1 2400 D87675 1 3252 D87675 1 3329 D87675 1 3449 D87675 1 3768 D87675 1 4424 D87675 1 5028 D87675 1 5235 D87675 1 5331 D87675 1 6606 D87675 1 6876 D87675 1 6920 D87675 1 7290 D87675 1 7595 D87675 1 7626 D87675 1 7754 D87675 1 8495 D87675 1 9122 D87675 1 9146 D87675 1 9180 D87675 1 9246 D87675 1 9327 D87675 1 9364 D87675 1 9807 D87675 1 10080 D87675 1 10427 D87675 1 10446 D87675 1 11251 D87675 1 11595 D87675 1 11611 D87675 1 11772 D87675 1 12071 D87675 1 12148 D87675 1 12358 D87675 1 12812 D87675 1 12887 D87675 1 13245 D87675 1 13263 D87675 1 14188 D87675 1 14395 D87675 1 14976 D87675 1 15529 D87675 1 16194 D87675 1 16285 D87675 1 16495 D87675 1 16962 D87675 1 17002 D87675 1 17325 D87675 1 17420 D87675 1 17671 D87675 1 18137 D87675 1 18653 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D87675 1 48184 D87675 1 48201 D87675 1 48291 D87675 1 48433 D87675 1 48612 D87675 1 49018 D87675 1 49286 D87675 1 50571 D87675 1 50653 D87675 1 50839 D87675 1 50983 D87675 1 51195 D87675 1 51316 D87675 1 51327 D87675 1 51558 D87675 1 51569 D87675 1 51766 D87675 1 51810 D87675 1 52391 D87675 1 52479 D87675 1 53037 D87675 1 53144 D87675 1 53631 D87675 1 53662 D87675 1 54084 D87675 1 54374 D87675 1 54525 D87675 1 54688 D87675 1 54735 67 D87675 2 712 D87675 2 1094 D87675 2 1422 D87675 2 2140 D87675 2 2409 D87675 2 2510 D87675 2 2963 D87675 2 3627 D87675 2 3740 D87675 2 4038 D87675 2 4454 D87675 2 4818 D87675 2 4850 D87675 2 5019 D87675 2 5060 D87675 2 5127 D87675 2 5138 D87675 2 5191 D87675 2 5313 D87675 2 5479 D87675 2 5545 D87675 2 5575 D87675 2 5720 D87675 2 6155 D87675 2 7071 D87675 2 7671 D87675 2 7785 D87675 2 7919 D87675 2 8206 D87675 2 8460 D87675 2 9171 D87675 2 9347 D87675 2 9656 D87675 2 9813 D87675 2 11007 D87675 2 11097 D87675 2 11716 D87675 2 13225 D87675 2 13715 D87675 2 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D87675 3 30391 D87675 3 31175 D87675 3 31598 D87675 3 31907 D87675 3 32149 D87675 3 32275 D87675 3 32441 D87675 3 32468 D87675 3 32773 D87675 3 32873 D87675 3 33091 D87675 3 33389 D87675 3 33492 D87675 3 33790 D87675 3 33930 D87675 3 33938 D87675 3 33952 D87675 3 34283 D87675 3 34376 D87675 3 34685 D87675 3 34734 D87675 3 35904 D87675 3 36087 D87675 3 36284 D87675 3 36538 75 D87675 4 615 D87675 4 671 D87675 4 693 D87675 4 704 D87675 4 1510 D87675 4 1619 D87675 4 1647 34 D87675 5 258 D87675 5 367 D87675 5 807 D87675 5 1641 D87675 5 2017 D87675 5 2021 D87675 5 2243 D87675 5 2368 D87675 5 2408 D87675 5 2446 D87675 5 2644 D87675 5 2853 D87675 5 3014 D87675 5 3217 D87675 5 3420 D87675 5 3534 D87675 5 3850 D87675 5 3863 D87675 5 4096 D87675 5 4154 D87675 5 4387 D87675 5 4405 D87675 5 4782 D87675 5 4937 D87675 5 5021 D87675 5 5088 D87675 5 5134 D87675 5 5192 D87675 5 5214 D87675 5 5275 D87675 5 5563 D87675 5 6211 D87675 5 6659 D87675 5 6750 D87675 5 7154 D87675 5 7201 D87675 5 7334 D87675 5 7421 D87675 5 8068 D87675 5 8728 D87675 5 8896 D87675 5 8952 D87675 5 9196 D87675 5 9290 D87675 5 10049 D87675 5 10356 D87675 5 10817 D87675 5 10911 D87675 5 11348 D87675 5 11368 D87675 5 11968 D87675 5 11972 D87675 5 12454 D87675 5 12520 D87675 5 13082 D87675 5 13491 D87675 5 14068 D87675 5 14090 D87675 5 14324 D87675 5 14442 D87675 5 14579 D87675 5 14903 D87675 5 16467 D87675 5 16854 D87675 5 18380 D87675 5 18422 D87675 5 18631 D87675 5 19300 D87675 5 19452 D87675 5 19511 D87675 5 19549 D87675 5 20031 D87675 5 20312 D87675 5 20546 D87675 5 20913 D87675 5 21064 D87675 5 21571 D87675 5 21617 D87675 5 22305 D87675 5 22886 D87675 5 23161 D87675 5 23246 D87675 5 23255 D87675 5 23429 D87675 5 23840 D87675 5 24195 D87675 5 24393 D87675 5 24436 D87675 5 24508 D87675 5 24822 D87675 5 25215 D87675 5 25682 D87675 5 25701 D87675 5 25886 D87675 5 26060 D87675 5 26334 D87675 5 26928 D87675 5 27041 D87675 5 27752 D87675 5 27756 D87675 5 27784 D87675 5 27926 D87675 5 27948 D87675 5 27998 D87675 5 28020 D87675 5 28070 D87675 5 28092 D87675 5 28274 D87675 5 28460 D87675 5 28850 2 D87675 6 300 D87675 6 325 D87675 6 382 D87675 6 450 D87675 6 798 D87675 6 838 D87675 6 898 D87675 6 1877 D87675 6 2124 D87675 6 2442 D87675 6 2449 D87675 6 2633 D87675 6 2731 D87675 6 2738 D87675 6 3236 D87675 6 3369 D87675 6 3415 D87675 6 3448 D87675 6 3483 D87675 6 3563 D87675 6 3825 D87675 6 3895 D87675 6 4401 D87675 6 4766 D87675 6 5037 D87675 6 5109 D87675 6 5558 D87675 6 5576 D87675 6 6074 D87675 6 6132 D87675 6 6225 D87675 6 6281 D87675 6 6314 D87675 6 6647 D87675 6 6900 D87675 6 7032 D87675 6 7431 D87675 6 7885 D87675 6 7936 D87675 6 8086 D87675 6 8606 D87675 6 8741 D87675 6 8783 D87675 6 8992 D87675 6 9084 D87675 6 9718 D87675 6 9741 D87675 6 9878 D87675 6 9892 D87675 6 10017 D87675 6 10138 D87675 6 10515 D87675 6 10938 D87675 6 11326 D87675 6 11455 D87675 6 11584 D87675 6 11677 D87675 6 11791 D87675 6 12002 D87675 6 12020 D87675 6 12951 D87675 6 13539 D87675 6 13594 D87675 6 13861 D87675 6 14582 D87675 6 15539 D87675 6 15623 D87675 6 15734 D87675 6 15784 D87675 6 16239 D87675 6 16361 D87675 6 16509 D87675 6 16539 D87675 6 16644 D87675 6 17072 D87675 6 17315 D87675 6 17389 D87675 6 17481 D87675 6 18029 D87675 6 18041 D87675 6 18178 D87675 6 18603 D87675 6 18821 D87675 6 18968 D87675 6 19077 D87675 6 19107 D87675 6 19406 D87675 6 19548 D87675 6 19835 D87675 6 19908 D87675 6 20096 D87675 6 20390 D87675 6 20652 D87675 6 20684 D87675 6 20753 D87675 6 20856 D87675 6 20951 51 D87675 7 452 D87675 7 520 D87675 7 661 D87675 7 805 D87675 7 1117 D87675 7 1145 D87675 7 1264 D87675 7 1699 D87675 7 2141 D87675 7 2484 171 D87675 8 399 D87675 8 530 D87675 8 588 D87675 8 644 D87675 8 674 D87675 8 682 D87675 8 908 D87675 8 992 D87675 8 1084 D87675 8 1088 D87675 8 1297 D87675 8 1482 D87675 8 1650 D87675 8 1663 D87675 8 1718 D87675 8 1959 D87675 8 2226 D87675 8 2611 D87675 8 2699 D87675 8 3353 D87675 8 3795 D87675 8 3863 D87675 8 4033 D87675 8 4460 D87675 8 4597 D87675 8 4618 D87675 8 5358 D87675 8 5482 D87675 8 5751 D87675 8 6441 D87675 8 6511 D87675 8 6604 D87675 8 6811 D87675 8 7064 D87675 8 7853 D87675 8 8194 D87675 8 8239 D87675 8 8513 D87675 8 8877 D87675 8 9441 D87675 8 9837 D87675 8 9898 D87675 8 10433 D87675 8 10476 D87675 8 10915 D87675 8 10978 D87675 8 11211 D87675 8 11952 D87675 8 11977 D87675 8 12393 D87675 8 12747 D87675 8 13521 D87675 8 13923 18 D87675 9 261 D87675 9 936 D87675 9 963 D87675 9 2532 D87675 9 2810 D87675 9 4104 D87675 9 4162 D87675 9 4280 D87675 9 4296 D87675 9 4782 D87675 9 4864 D87675 9 5154 D87675 9 5187 D87675 9 5339 D87675 9 6185 118 D87675 10 518 D87675 10 556 97 D87675 11 791 D87675 11 1254 D87675 11 1344 D87675 11 1753 D87675 11 1954 D87675 11 2085 D87675 11 3117 D87675 11 3214 D87675 11 3383 D87675 11 3644 D87675 11 3729 D87675 11 3862 D87675 11 4070 D87675 11 4255 D87675 11 4604 D87675 11 4675 D87675 11 5924 D87675 11 6188 D87675 11 6659 D87675 11 6810 D87675 11 6812 D87675 11 7693 D87675 11 8058 D87675 11 8139 D87675 11 8150 D87675 11 8158 D87675 11 8248 D87675 11 8454 D87675 11 8464 D87675 11 8494 D87675 11 8633 D87675 11 8715 D87675 11 8939 D87675 11 9000 D87675 11 9462 D87675 11 9565 D87675 11 9959 D87675 11 10166 D87675 11 10475 D87675 11 10587 D87675 11 11211 D87675 11 11278 D87675 11 11568 D87675 11 11582 D87675 11 11806 D87675 11 11909 D87675 11 12009 D87675 11 12023 D87675 11 12090 D87675 11 12179 D87675 11 12334 D87675 11 12479 D87675 11 12493 D87675 11 12541 D87675 11 12742 D87675 11 12865 D87675 11 13889 D87675 11 13900 D87675 11 13962 D87675 11 14152 D87675 11 14806 D87675 11 15191 D87675 11 15688 D87675 11 15928 D87675 11 15998 D87675 11 16144 D87675 11 16363 D87675 11 16431 D87675 11 16468 D87675 11 16558 D87675 11 18166 D87675 11 18625 D87675 11 18690 D87675 11 19136 D87675 11 19194 91 D87675 12 99 D87675 12 134 D87675 12 362 D87675 12 653 D87675 12 812 34 D87675 13 3 D87675 13 65 D87675 13 494 D87675 13 510 D87675 13 707 D87675 13 902 D87675 13 1120 D87675 13 1407 D87675 13 1875 D87675 13 1899 D87675 13 2348 D87675 13 2363 D87675 13 2399 D87675 13 3260 D87675 13 3429 D87675 13 3976 D87675 13 4460 D87675 13 4470 D87675 13 5590 D87675 13 5844 D87675 13 6474 D87675 13 6666 D87675 13 6986 D87675 13 7282 D87675 13 7341 D87675 13 7553 D87675 13 7830 D87675 13 8657 D87675 13 9068 D87675 13 9344 D87675 13 9409 D87675 13 9465 D87675 13 10022 D87675 13 10100 D87675 13 10160 D87675 13 10174 D87675 13 10595 D87675 13 10778 D87675 13 11187 D87675 13 11205 D87675 13 11356 D87675 13 11559 D87675 13 12062 D87675 13 12231 D87675 13 12465 D87675 13 12469 D87675 13 12609 D87675 13 12773 D87675 13 12881 D87675 13 13120 D87675 13 13462 D87675 13 13560 D87675 13 13763 D87675 13 13839 D87675 13 13927 D87675 13 14036 D87675 13 14072 D87675 13 14144 D87675 13 14372 D87675 13 14490 D87675 13 14721 D87675 13 14899 D87675 13 15256 D87675 13 15280 D87675 13 15449 D87675 13 15552 D87675 13 15611 D87675 13 15778 D87675 13 16027 D87675 13 16282 D87675 13 16314 D87675 13 17232 D87675 13 17389 D87675 13 17656 D87675 13 17923 D87675 13 18014 D87675 13 18253 D87675 13 18686 D87675 13 19007 D87675 13 19076 D87675 13 19922 D87675 13 20111 D87675 13 20324 D87675 13 20594 D87675 13 20958 D87675 13 21003 D87675 13 21105 D87675 13 21238 D87675 13 21332 D87675 13 21377 D87675 13 21415 D87675 13 21680 D87675 13 21739 D87675 13 21933 D87675 13 22147 D87675 13 22224 D87675 13 22728 D87675 13 23029 D87675 13 23099 D87675 13 23161 D87675 13 23606 D87675 13 24570 D87675 13 25364 D87675 13 25430 D87675 13 25638 D87675 13 25919 D87675 13 26133 D87675 13 26636 D87675 13 26724 D87675 13 28002 D87675 13 28259 D87675 13 29015 D87675 13 29031 D87675 13 29406 D87675 13 29532 D87675 13 29566 D87675 13 29853 D87675 13 29937 D87675 13 30084 D87675 13 30317 D87675 13 30953 D87675 13 31484 D87675 13 31510 D87675 13 31922 D87675 13 31939 D87675 13 32250 D87675 13 33389 D87675 13 33642 D87675 13 33848 D87675 13 34255 D87675 13 34656 D87675 13 35239 D87675 13 35438 D87675 13 35632 D87675 13 35878 D87675 13 35963 D87675 13 36026 D87675 13 36769 D87675 13 37439 D87675 13 37443 D87675 13 37589 D87675 13 37636 D87675 13 37653 D87675 13 38186 D87675 13 38358 D87675 13 38504 D87675 13 38627 D87675 13 38980 D87675 13 39425 D87675 13 39448 D87675 13 39678 D87675 13 40331 D87675 13 40409 D87675 13 40681 D87675 13 40886 D87675 13 40962 D87675 13 41035 D87675 13 41677 D87675 13 41727 D87675 13 42553 6 D87675 14 36 D87675 14 57 D87675 14 100 D87675 14 155 D87675 14 320 D87675 14 668 D87675 14 1042 D87675 14 1361 D87675 14 1377 D87675 14 1744 D87675 14 1969 D87675 14 2175 D87675 14 3022 D87675 14 4234 D87675 14 4287 D87675 14 4353 D87675 14 4641 D87675 14 4724 D87675 14 4750 D87675 14 4862 D87675 14 4874 D87675 14 4898 D87675 14 5276 D87675 14 5913 D87675 14 5924 D87675 14 6085 D87675 14 6414 96 D87675 15 364 D87675 15 421 D87675 15 1246 D87675 15 1300 D87675 15 1374 D87675 15 1411 D87675 15 1487 D87675 15 1585 D87675 15 1874 D87675 15 2528 D87675 15 2549 D87675 15 2620 D87675 15 2975 D87675 15 3339 D87675 15 4159 D87675 15 4281 D87675 15 4934 D87675 15 4990 D87675 15 5058 D87675 15 5293 D87675 15 5404 D87675 15 5836 D87675 15 6181 D87675 15 6226 D87675 15 6915 15 D87675 16 225 D87675 16 811 D87675 16 1073 D87675 16 1150 D87675 16 1448 D87675 16 1934 D87675 16 2163 D87675 16 2175 D87675 16 2615 D87675 16 2910 D87675 16 3152 D87675 16 3381 D87675 16 3389 D87675 16 3579 D87675 16 4212 D87675 16 5065 D87675 16 5101 D87675 16 5105 D87675 16 5498 D87675 16 5528 100 D87675 17 3 D87675 17 448 D87675 17 463 D87675 17 1198 D87675 17 1294 D87675 17 2359 D87675 17 3376 D87675 17 4295 D87675 17 4751 D87675 17 4793 D87675 17 4935 D87675 17 5081 D87675 17 5127 D87675 17 5780 D87675 17 5947 D87675 17 6197 D87675 17 6201 D87675 17 6443 D87675 17 6688 D87675 17 7058 D87675 17 7235 D87675 17 7411 D87675 17 7529 D87675 17 7597 D87675 17 7615 D87675 17 8775 D87675 17 9118 D87675 17 9217 37 HUMPIM1A 3 41 31 HUMPIM1A 4 29 HUMPIM1A 4 96 HUMPIM1A 4 678 HUMPIM1A 4 863 HUMPIM1A 4 1120 HUMPIM1A 4 1302 HUMPIM1A 4 1337 HUMPIM1A 4 1470 93 HUMPIM1A 5 131 HUMPIM1A 5 197 HUMPIM1A 5 405 HUMPIM1A 5 413 HUMPIM1A 5 417 HUMPIM1A 5 489 6 HSTCRT3D 1 14 HSTCRT3D 1 563 HSTCRT3D 1 703 HSTCRT3D 1 1620 HSTCRT3D 1 1682 108 HSTCRT3D 2 48 HSTCRT3D 2 104 HSTCRT3D 2 109 HSTCRT3D 2 218 HSTCRT3D 2 315 36 HSTCRT3D 3 108 3 HSTCRT3D 4 37 HSTCRT3D 4 127 40 HSCYTOK17 2 241 HSCYTOK17 2 369 2 HSCYTOK17 3 4 HSCYTOK17 3 277 HSCYTOK17 3 552 280 HSCYTOK17 4 178 HSCYTOK17 4 190 HSCYTOK17 4 401 55 HSCYTOK17 7 123 HSCYTOK17 7 694 99 HUMTRPY1B 1 45 HUMTRPY1B 1 57 135 HUMTRPY1B 2 40 2 HUMTRPY1B 3 20 HUMTRPY1B 3 73 AB005803 1 53 AB005803 1 327 AB005803 1 484 AB005803 1 639 AB005803 1 1019 AB005803 1 1071 AB005803 1 1211 AB005803 1 1339 AB005803 1 1442 AB005803 1 1457 AB005803 1 1484 AB005803 1 1536 AB005803 1 1579 AB005803 1 1610 AB005803 1 1841 AB005803 1 2080 25 AB005803 2 196 AB005803 2 240 AB005803 2 296 AB005803 2 417 AB005803 2 501 115 AB005803 3 260 AB005803 3 264 AB005803 3 753 AB005803 3 795 AB005803 3 1140 15 AB005803 4 147 AB005803 4 511 AB005803 4 753 AB005803 4 832 AB005803 4 882 13 AB005803 5 210 AB005803 5 446 AB005803 5 825 AB005803 5 1425 AB005803 5 1474 AB005803 5 1676 28 AB005803 6 93 AB005803 6 465 AB005803 6 885 AB005803 6 910 AB005803 6 1473 AB005803 6 1548 AB005803 6 1658 88 HSDNAAMHI 1 89 HSDNAAMHI 1 102 105 HSDNAAMHI 2 22 222 HSDNAAMHI 3 44 HSDNAAMHI 3 134 HSDNAAMHI 3 172 HSDNAAMHI 3 223 48 HSDNAAMHI 6 21 HSDNAAMHI 6 53 HSDNAAMHI 6 179 HSDNAAMHI 6 472 HSDNAAMHI 6 681 HSDNAAMHI 6 1040 HSDNAAMHI 6 1319 HSDNAAMHI 6 1362 HSDNAAMHI 6 1895 HSDNAAMHI 6 2013 HSDNAAMHI 6 2211 HSDNAAMHI 6 2474 HSDNAAMHI 6 2571 HSDNAAMHI 6 2761 115 HSDNAAMHI 7 3 HSDNAAMHI 7 150 HSDNAAMHI 7 166 6 HSDNAAMHI 8 19 22 HSDNAAMHI 10 456 274 HSDNAMIA 2 413 HSDNAMIA 2 615 HSDNAMIA 2 764 94 HSDNAMIA 3 97 178 HSU75285 2 212 HSU75285 2 413 HSU75285 2 1244 HSU75285 2 1565 2 HSU75285 3 198 HSU75285 3 224 HSU75285 3 494 HSU75285 3 556 HSU75285 3 629 HSU75285 3 671 HSU75285 3 992 HSU75285 3 1136 HSU75285 3 1408 HSU75285 3 1470 HSU75285 3 2098 HSU75285 3 2302 HSU75285 3 2541 HSU75285 3 2676 HSU75285 3 2859 HSU75285 3 3136 HSU75285 3 3335 HSU75285 3 3427 HSU75285 3 4076 HSU75285 3 4394 HSU75285 3 5020 HSU75285 3 5317 HSU75285 3 5554 HSU75285 3 5589 HSU75285 3 5820 HSU75285 3 5888 HSU75285 3 6019 HSU75285 3 6206 HSU75285 3 6531 HSU75285 3 6627 46 HSCOSE 1 825 HSCOSE 1 1132 103 HSLPAPGEN 1 109 HSLPAPGEN 1 818 HSLPAPGEN 1 899 HSLPAPGEN 1 936 HSLPAPGEN 1 1028 HSLPAPGEN 1 1054 55 HSU56438 1 381 HSU56438 1 533 HSU56438 1 828 HSU56438 1 1015 HSU56438 1 1057 HSU56438 1 1205 HSU56438 1 1209 HSU56438 1 1409 HSU56438 1 1846 HSU56438 1 2064 HSU56438 1 2615 2 HSU08198 1 92 HSU08198 1 123 64 HSU08198 3 22 36 HSU08198 4 75 78 HSU08198 6 33 36 HSCFOS 1 212 HSCFOS 1 404 82 HSCFOS 2 299 HSCFOS 2 364 HSCFOS 2 368 HSCFOS 2 378 118 D89501 1 252 D89501 1 285 D89501 1 1200 D89501 1 1251 D89501 1 1607 D89501 1 1919 D89501 1 1982 D89501 1 2103 D89501 1 2167 D89501 1 2611 D89501 1 2787 D89501 1 2812 D89501 1 3117 D89501 1 3283 D89501 1 4003 D89501 1 4039 D89501 1 4336 100 HUMGARE 1 656 HUMGARE 1 714 57 HUMGARE 2 3 HUMGARE 2 133 6 HUMGARE 3 207 2 HUMGARE 4 14 HUMGARE 4 88 HUMGARE 4 94 HUMGARE 4 135 HUMGARE 4 140 HUMCRPGA 1 39 HUMCRPGA 1 127 HUMCRPGA 1 158 HUMCRPGA 1 177 HUMCRPGA 1 209 HUMCRPGA 1 213 57 HSNGALGEN 1 65 HSNGALGEN 1 253 268 HSNGALGEN 2 617 HSNGALGEN 2 867 2 HSNGALGEN 3 15 9 HSNGALGEN 5 694 18 HSU43415 1 206 HSU43415 1 437 HSU43415 1 657 HSU43415 1 1227 HSU43415 1 1499 HSU43415 1 2118 94 HUMHMG14A 2 26 40 HUMHMG14A 3 48 HUMHMG14A 4 114 HUMHMG14A 4 375 HUMHMG14A 4 449 HUMHMG14A 4 573 HUMHMG14A 4 604 HUMHMG14A 4 715 HUMHMG14A 4 741 HUMHMG14A 4 1040 HUMHMG14A 4 1094 HUMHMG14A 4 1331 HUMHMG14A 4 1391 HUMHMG14A 4 1410 HUMHMG14A 4 1422 HUMHMG14A 4 1453 HUMHMG14A 4 1566 HUMHMG14A 4 1898 HUMHMG14A 4 1925 HUMHMG14A 4 2114 HUMHMG14A 4 2121 HUMHMG14A 4 2296 HUMHMG14A 4 2460 HUMHMG14A 4 2475 HUMHMG14A 4 2764 HUMHMG14A 4 2964 79 HUMHMG14A 5 6 HUMHMG14A 5 145 HUMHMG14A 5 187 HUMHMG14A 5 195 HUMHMG14A 5 416 HUMHMG14A 5 713 HUMHMG14A 5 1119 HUMHMG14A 5 1161 HUMHMG14A 5 1436 HUMHMG14A 5 1479 HUMHMG14A 5 1841 HUMHMG14A 5 1880 HUMHMG14A 5 1884 67 HUMPCNA 1 349 HUMPCNA 1 617 2 HUMPCNA 2 53 60 HUMPCNA 3 571 HUMPCNA 3 653 HUMPCNA 3 875 22 HUMPCNA 4 59 HUMPCNA 4 100 HUMPCNA 4 1011 HUMPCNA 4 1262 HUMPCNA 4 1472 HUMPCNA 4 1497 13 HUMHMGIY 1 50 HUMHMGIY 1 124 HUMHMGIY 1 489 HUMHMGIY 1 835 HUMHMGIY 1 1061 HUMHMGIY 1 1613 HUMHMGIY 1 1673 HUMHMGIY 1 1761 115 HUMHMGIY 2 142 HUMHMGIY 2 231 HUMHMGIY 2 471 HUMHMGIY 2 557 HUMHMGIY 2 588 HUMHMGIY 2 621 34 HUMHMGIY 3 3 HUMHMGIY 3 149 HUMHMGIY 3 178 HUMHMGIY 3 358 HUMHMGIY 3 691 HUMHMGIY 3 772 HUMHMGIY 3 1090 HUMHMGIY 3 1103 43 HSHOX51 1 77 HSHOX51 1 148 HSHOX51 1 340 HSHOX51 1 344 HSHOX51 1 348 HSHOX51 1 362 HSHOX51 1 466 18 HSSGK 2 192 2 HSSGK 7 128 2 HSSGK 8 201 HSSGK 8 205 HSSGK 8 240 HSSGK 8 274 109 HSSGK 9 293 HSSGK 9 393 97 HSSGK 11 223 HSSGK 11 227 HSSGK 11 303 130 HSU30787 1 516 2 HSU30787 5 73 91 HSU30787 6 195 HSU30787 6 218 HSU30787 6 297 43 HSU30787 8 14 HSU30787 8 33 2 HUMGLUT4B 1 113 HUMGLUT4B 1 645 HUMGLUT4B 1 892 HUMGLUT4B 1 954 154 HUMGLUT4B 2 48 HUMGLUT4B 5 74 91 HUMGLUT4B 9 52 16 HUMGLUT4B 10 40 HUMGLUT4B 10 112 HUMGLUT4B 10 187 58 HUMAPOE4 1 450 HUMAPOE4 1 696 HUMAPOE4 1 948 HUMAPOE4 1 1029 177 HUMTRHYAL 1 147 HUMTRHYAL 1 208 HUMTRHYAL 1 586 HUMTRHYAL 1 694 43 HSPPTII 1 34 85 HSPPTII 2 213 HSPPTII 2 315 HSPPTII 2 380 HSPPTII 2 430 HSPPTII 2 711 HSPPTII 2 1328 HSPPTII 2 1366 HSPPTII 2 1486 HSPPTII 2 1501 HSPPTII 2 1587 HSPPTII 2 1797 53 HSU51899 1 131 HSU51899 1 945 HSU51899 1 1618 HSU51899 1 1738 HSU51899 1 2074 7 HSU51899 2 58 HSU51899 2 155 HSU51899 2 719 HSU51899 2 733 HSU51899 2 1050 HSU51899 2 1087 13 HUMANT2X 1 186 HUMANT2X 1 683 HUMANT2X 1 736 112 HUMANT2X 2 175 105 HUMANT2X 3 170 HUMANT2X 3 287 33 HUMCHYMASE 1 427 HUMCHYMASE 1 562 24 HUMCHYMASE 4 91 HUMCHYMASE 4 99 HUMCHYMASE 4 184 HUMCHYMASE 4 251 49 HSRING3GE 1 26 HSRING3GE 1 346 HSRING3GE 1 386 HSRING3GE 1 513 52 HSRING3GE 2 28 HSRING3GE 2 113 HSRING3GE 2 171 HSRING3GE 2 195 HSRING3GE 2 445 121 HSRING3GE 5 457 49 HSRING3GE 6 75 HSRING3GE 6 133 22 HSRING3GE 7 30 16 HSRING3GE 8 1027 HSRING3GE 8 1204 HSRING3GE 8 1208 HSRING3GE 8 1394 2 AF027807 1 492 AF027807 1 535 AF027807 1 583 AF027807 1 764 61 AF027807 2 129 AF027807 2 396 AF027807 2 496 AF027807 2 528 AF027807 2 547 AF027807 2 934 7 AF027807 4 313 AF027807 4 333 AF027807 4 586 AF027807 4 774 AF027807 4 901 10 AF027807 5 105 AF027807 5 160 AF027807 5 282 AF027807 5 327 AF027807 5 521 AF027807 5 738 AF027807 5 883 67 HUMPCBD 1 59 HUMPCBD 1 862 HUMPCBD 1 1426 HUMPCBD 1 1740 HUMPCBD 1 2270 181 HUMPCBD 3 357 HUMPCBD 3 420 HUMPCBD 3 436 HUMPCBD 3 1067 58 HSHAP1 1 69 72 HSHAP1 2 368 13 HUMTNFX 1 226 HUMTNFX 1 349 HUMTNFX 1 473 HUMTNFX 1 564 244 HUMTNFX 2 51 HUMTNFX 2 117 120 HUMTNFX 3 89 HUMTNFX 3 170 39 HUMAGAL 1 36 HUMAGAL 1 76 HUMAGAL 1 80 HUMAGAL 1 324 HUMAGAL 1 625 HUMAGAL 1 962 HUMAGAL 1 993 HUMAGAL 1 998 HUMAGAL 1 1422 33 HUMAGAL 2 92 HUMAGAL 2 254 HUMAGAL 2 448 2 HUMAGAL 3 77 HUMAGAL 3 302 HUMAGAL 3 320 37 HUMAGAL 4 180 78 HUMAGAL 5 123 HUMAGAL 5 134 HUMAGAL 5 172 HUMAGAL 5 194 HUMAGAL 5 362 HUMAGAL 5 491 HUMAGAL 5 495 133 HUMAGAL 6 101 HUMAGAL 6 501 HUMAGAL 6 649 HUMAGAL 6 870 HUMAGAL 6 886 HUMAGAL 6 1347 HUMAGAL 6 1590 HUMAGAL 6 1780 HUMAGAL 6 1872 HUMAGAL 6 2187 HUMAGAL 6 2500 25 HUMAGAL 7 192 HUMAGAL 7 270 HUMAGAL 7 568 HUMAGAL 7 733 HUMAGAL 7 981 HUMAGAL 7 997 HUMAGAL 7 1579 HUMAGAL 7 1700 34 HUMFIXG 1 133 HUMFIXG 1 137 HUMFIXG 1 258 HUMFIXG 1 472 HUMFIXG 1 484 HUMFIXG 1 1044 HUMFIXG 1 1180 HUMFIXG 1 1358 HUMFIXG 1 1495 HUMFIXG 1 1542 HUMFIXG 1 1742 HUMFIXG 1 1956 HUMFIXG 1 1961 HUMFIXG 1 2003 HUMFIXG 1 2012 HUMFIXG 1 2378 HUMFIXG 1 2559 HUMFIXG 1 2706 HUMFIXG 1 2751 HUMFIXG 1 2868 HUMFIXG 1 2914 HUMFIXG 1 2992 HUMFIXG 1 3227 HUMFIXG 1 3268 HUMFIXG 1 3612 HUMFIXG 1 3984 HUMFIXG 1 4008 HUMFIXG 1 4060 HUMFIXG 1 4283 HUMFIXG 1 4315 HUMFIXG 1 4554 HUMFIXG 1 4906 HUMFIXG 1 5101 HUMFIXG 1 5302 HUMFIXG 1 5591 HUMFIXG 1 5950 84 HUMFIXG 2 101 16 HUMFIXG 3 51 HUMFIXG 3 185 HUMFIXG 3 987 HUMFIXG 3 1278 HUMFIXG 3 1354 HUMFIXG 3 2062 HUMFIXG 3 2929 HUMFIXG 3 3570 27 HUMFIXG 4 3 HUMFIXG 4 192 HUMFIXG 4 258 HUMFIXG 4 458 HUMFIXG 4 1085 HUMFIXG 4 1101 HUMFIXG 4 1535 HUMFIXG 4 1575 HUMFIXG 4 2179 HUMFIXG 4 3051 HUMFIXG 4 3631 HUMFIXG 4 3916 HUMFIXG 4 3951 HUMFIXG 4 4061 HUMFIXG 4 4428 HUMFIXG 4 4765 HUMFIXG 4 4963 HUMFIXG 4 5207 HUMFIXG 4 5547 HUMFIXG 4 6040 HUMFIXG 4 6550 HUMFIXG 4 6694 HUMFIXG 4 6778 6 HUMFIXG 5 373 HUMFIXG 5 1477 HUMFIXG 5 1485 HUMFIXG 5 1881 HUMFIXG 5 1990 HUMFIXG 5 2536 24 HUMFIXG 6 15 HUMFIXG 6 56 HUMFIXG 6 98 HUMFIXG 6 135 HUMFIXG 6 337 HUMFIXG 6 607 HUMFIXG 6 785 HUMFIXG 6 830 HUMFIXG 6 1268 HUMFIXG 6 1543 HUMFIXG 6 1622 HUMFIXG 6 1721 HUMFIXG 6 1755 HUMFIXG 6 2606 HUMFIXG 6 3688 HUMFIXG 6 3714 HUMFIXG 6 4291 HUMFIXG 6 4336 HUMFIXG 6 4852 HUMFIXG 6 4933 HUMFIXG 6 5501 HUMFIXG 6 5648 HUMFIXG 6 5652 HUMFIXG 6 5689 HUMFIXG 6 5713 HUMFIXG 6 5733 HUMFIXG 6 5786 HUMFIXG 6 5811 HUMFIXG 6 5836 HUMFIXG 6 6379 HUMFIXG 6 6870 HUMFIXG 6 6963 HUMFIXG 6 7159 HUMFIXG 6 7405 HUMFIXG 6 8341 HUMFIXG 6 8611 HUMFIXG 6 9060 67 HUMFIXG 7 372 HUMFIXG 7 584 51 AF009356 1 240 AF009356 1 403 AF009356 1 435 2 AF009356 2 169 AF009356 2 177 AF009356 2 181 2 AF009356 3 163 6 AF009356 4 122 AF009356 4 305 AF009356 4 538 AF009356 4 562 AF009356 4 713 AF009356 4 734 AF009356 4 888 70 HSMECDAG 1 62 HSMECDAG 1 411 HSMECDAG 1 662 HSMECDAG 1 755 HSMECDAG 1 814 169 HSMECDAG 2 66 HSMECDAG 2 70 HSMECDAG 2 75 HSMECDAG 2 79 HSMECDAG 2 83 HSMECDAG 2 98 73 HSMECDAG 4 65 HSMECDAG 4 105 HSMECDAG 4 123 HSMECDAG 4 195 HSMECDAG 4 203 HSMECDAG 4 235 HSMECDAG 4 386 121 HSMECDAG 6 133 61 HSU12709 1 45 108 HSU12709 3 174 14 HUMANFA 1 77 118 HUMANFA 2 333 HUMANFA 2 450 HUMANFA 2 554 HUMANFA 2 645 HUMANFA 2 991 157 HSERPG 1 82 198 HSERPG 3 90 HSERPG 3 259 112 HUMTPA 1 504 HUMTPA 1 522 HUMTPA 1 692 HUMTPA 1 860 HUMTPA 1 1290 HUMTPA 1 1596 205 HUMTPA 2 219 HUMTPA 2 717 HUMTPA 2 1113 HUMTPA 2 1519 HUMTPA 2 2066 HUMTPA 2 2205 114 HUMTPA 3 59 HUMTPA 3 156 HUMTPA 3 458 HUMTPA 3 542 9 HUMTPA 4 7 HUMTPA 4 171 HUMTPA 4 301 6 HUMTPA 5 149 HUMTPA 5 185 HUMTPA 5 271 HUMTPA 5 548 HUMTPA 5 600 HUMTPA 5 612 HUMTPA 5 715 HUMTPA 5 960 HUMTPA 5 1164 HUMTPA 5 1440 HUMTPA 5 1537 HUMTPA 5 1893 HUMTPA 6 108 HUMTPA 6 317 HUMTPA 6 490 HUMTPA 6 941 HUMTPA 6 981 HUMTPA 6 1026 HUMTPA 6 1139 HUMTPA 6 1147 HUMTPA 6 1380 69 HUMTPA 7 406 2 HUMTPA 8 153 HUMTPA 8 240 HUMTPA 8 466 HUMTPA 8 578 HUMTPA 8 582 HUMTPA 8 657 HUMTPA 8 772 HUMTPA 8 819 HUMTPA 8 879 141 HUMTPA 11 473 HUMTPA 11 538 HUMTPA 11 561 114 HUMTPA 12 376 HUMTPA 12 394 HUMTPA 12 729 HUMTPA 12 993 HUMTPA 12 1365 HUMTPA 12 1387 HUMTPA 12 1519 HUMTPA 12 1575 HUMTPA 12 1644 HUMTPA 12 1706 HUMTPA 12 1778 HUMTPA 12 1786 HUMTPA 12 1873 HUMTPA 12 2031 HUMTPA 12 2056 HUMTPA 12 2130 HUMTPA 12 2171 112 AC004022 1 14 AC004022 1 228 AC004022 1 696 AC004022 1 1006 AC004022 1 1058 AC004022 1 1466 AC004022 1 1561 AC004022 1 1784 AC004022 1 2513 AC004022 1 2656 AC004022 1 2688 AC004022 1 2825 AC004022 1 2850 AC004022 1 2875 AC004022 1 3146 AC004022 1 3163 AC004022 1 3218 AC004022 1 3319 AC004022 1 3686 AC004022 1 3702 AC004022 1 3763 AC004022 1 3883 AC004022 1 4161 AC004022 1 4212 AC004022 1 4416 AC004022 1 4558 AC004022 1 4607 AC004022 1 5079 AC004022 1 5130 AC004022 1 5156 AC004022 1 5459 AC004022 1 5463 2 AC004022 2 3 AC004022 2 7 AC004022 2 342 AC004022 2 528 AC004022 2 1453 AC004022 2 1458 66 AC004022 3 248 AC004022 3 368 AC004022 3 725 31 AC004022 4 1086 AC004022 4 1554 AC004022 4 1619 AC004022 4 1658 AC004022 4 1838 AC004022 4 2115 AC004022 4 2458 AC004022 4 2523 AC004022 4 2588 AC004022 4 3660 111 AC004022 5 84 AC004022 5 769 AC004022 5 788 AC004022 5 1045 AC004022 5 1062 AC004022 5 1149 AC004022 5 2837 AC004022 5 2851 AC004022 5 3217 5 AC004022 6 289 AC004022 6 330 AC004022 6 376 AC004022 6 428 AC004022 6 486 AC004022 6 663 AC004022 6 708 AC004022 6 989 AC004022 6 1386 AC004022 6 1510 AC004022 6 1521 77 AC004022 7 17 AC004022 7 95 AC004022 7 99 AC004022 7 461 AC004022 7 1298 AC004022 7 1394 AC004022 7 1547 AC004022 7 1592 AC004022 7 1703 AC004022 7 2114 AC004022 7 2960 AC004022 7 3043 AC004022 7 3169 AC004022 7 3186 AC004022 7 3225 AC004022 7 3784 AC004022 7 3798 40 AC004022 8 25 AC004022 8 476 AC004022 8 670 AC004022 8 999 AC004022 8 1028 AC004022 8 1354 AC004022 8 1726 AC004022 8 1922 AC004022 8 2647 AC004022 8 2955 AC004022 8 3058 28 HSGLTH1 2 48 94 HSGEBCMA 1 92 HSGEBCMA 1 158 HSGEBCMA 1 280 HSGEBCMA 1 428 HSGEBCMA 1 529 HSGEBCMA 1 686 HSGEBCMA 1 690 6 HSGEBCMA 2 11 HSGEBCMA 2 48 HSGEBCMA 2 151 HSGEBCMA 2 200 HSGEBCMA 2 795 51 AB005990 1 226 49 AB005990 2 275 2 AB005990 8 151 AB005990 8 155 61 HUMAPOCIA 1 50 HUMAPOCIA 1 136 HUMAPOCIA 1 264 HUMAPOCIA 1 268 HUMAPOCIA 1 296 HUMAPOCIA 1 341 HUMAPOCIA 1 804 HUMAPOCIA 1 880 78 HUMAPOCIA 2 33 HUMAPOCIA 2 260 HUMAPOCIA 2 278 HUMAPOCIA 2 425 HUMAPOCIA 2 676 HUMAPOCIA 2 1038 HUMAPOCIA 2 1056 HUMAPOCIA 2 1440 HUMAPOCIA 2 1736 HUMAPOCIA 2 1926 HUMAPOCIA 2 2484 HUMAPOCIA 2 2551 HUMAPOCIA 2 2770 HUMAPOCIA 2 2811 173 HSGLA 1 47 HSGLA 1 447 HSGLA 1 773 HSGLA 1 869 HSGLA 1 964 HSGLA 1 1097 HSGLA 1 1465 HSGLA 1 2047 HSGLA 1 2687 HSGLA 1 2774 HSGLA 1 2790 HSGLA 1 2892 HSGLA 1 3647 HSGLA 1 3665 578 HSGLA 2 1129 HSGLA 2 1436 HSGLA 2 1688 HSGLA 2 1713 HSGLA 2 1971 10 HSGLA 3 398 HSGLA 3 564 87 HSGLA 4 429 HSGLA 4 921 HSGLA 4 1454 HSGLA 4 1507 HSGLA 4 1675 7 HSGLA 5 65 HSGLA 5 75 HSGLA 5 101 HSGLA 5 159 10 HSU43901 1 34 HSU43901 1 67 HSU43901 1 78 HSU43901 1 189 HSU43901 1 288 HSU43901 1 332 HSU43901 1 339 3 HSU43901 2 14 HSU43901 2 164 HSU43901 2 1075 HSU43901 2 1334 HSU43901 2 1674 HSU43901 2 1915 HSU43901 2 1939 76 HSU43901 3 361 HSU43901 3 574 HSU43901 3 589 40 HSU43901 4 83 HSU43901 5 17 HSU43901 5 150 30 HUMCSPA 1 3 HUMCSPA 1 284 HUMCSPA 1 900 6 HUMCSPA 2 200 2 HUMCSPA 3 96 88 HUMCSPA 4 298 49 HUMSPERSYN 1 375 32 HUMSPERSYN 2 46 163 HUMSPERSYN 3 89 HUMSPERSYN 3 172 HUMSPERSYN 3 455 HUMSPERSYN 3 788 HUMSPERSYN 3 1649 HUMSPERSYN 3 1694 HUMSPERSYN 3 1889 175 HUMSPERSYN 4 48 HUMSPERSYN 4 330 HUMSPERSYN 4 385 75 HUMSPERSYN 6 38 HUMSPERSYN 6 131 HUMSPERSYN 6 377 HUMSPERSYN 6 422 HUMSPERSYN 6 440 166 HUMHLL4G 1 275 HUMHLL4G 1 575 88 HUMHLL4G 2 133 HUMHLL4G 2 459 HUMHLL4G 2 522 HUMHLL4G 2 539 HUMHLL4G 2 1308 HUMHLL4G 2 1326 HUMHLL4G 2 1361 2 HUMHLL4G 3 61 HUMHLL4G 3 545 HUMHLL4G 3 563 163 HUMN79E2 1 84 HUMN79E2 1 113 HUMN79E2 1 217 HUMN79E2 1 627 HUMN79E2 1 802 HUMN79E2 1 1063 HUMN79E2 1 1144 HUMN79E2 1 1402 HUMN79E2 1 1543 HUMN79E2 1 1870 HUMN79E2 1 1972 HUMN79E2 1 2403 HUMN79E2 1 2472 HUMN79E2 1 2676 HUMN79E2 1 4386 HUMN79E2 1 4678 HUMN79E2 1 4763 HUMN79E2 1 4822 HUMN79E2 1 4879 HUMN79E2 1 5024 HUMN79E2 1 5151 HUMN79E2 1 5582 HUMN79E2 1 5620 HUMN79E2 1 5845 HUMN79E2 1 6124 HUMN79E2 1 6656 HUMN79E2 1 7106 HUMN79E2 1 7603 HUMN79E2 1 8007 HUMN79E2 1 8026 HUMN79E2 1 8383 HUMN79E2 1 8695 HUMN79E2 1 8828 HUMN79E2 1 9392 HUMN79E2 1 9856 HUMN79E2 1 10301 HUMN79E2 1 10395 HUMN79E2 1 10513 HUMN79E2 1 11148 HUMN79E2 1 11172 HUMN79E2 1 11362 HUMN79E2 1 11431 HUMN79E2 1 11563 HUMN79E2 1 11955 HUMN79E2 1 11972 HUMN79E2 1 11978 HUMN79E2 1 12183 HUMN79E2 1 12252 HUMN79E2 1 12500 HUMN79E2 1 12873 HUMN79E2 1 12915 HUMN79E2 1 13129 HUMN79E2 1 13362 HUMN79E2 1 13613 HUMN79E2 1 13657 HUMN79E2 1 13876 HUMN79E2 1 13925 HUMN79E2 1 14243 HUMN79E2 1 14337 HUMN79E2 1 14389 HUMN79E2 1 14552 HUMN79E2 1 14672 HUMN79E2 1 14895 HUMN79E2 1 15038 HUMN79E2 1 15328 HUMN79E2 1 15511 HUMN79E2 1 15637 HUMN79E2 1 15754 HUMN79E2 1 15900 HUMN79E2 1 15965 HUMN79E2 1 16106 HUMN79E2 1 16198 HUMN79E2 1 16227 HUMN79E2 1 16323 HUMN79E2 1 16441 HUMN79E2 1 16624 HUMN79E2 1 16839 HUMN79E2 1 16857 HUMN79E2 1 16975 133 HSU96876 1 366 HSU96876 1 688 HSU96876 1 867 HSU96876 1 930 HSU96876 1 1169 HSU96876 1 1237 HSU96876 1 1285 HSU96876 1 1661 HSU96876 1 1798 HSU96876 1 1824 30 HSU96876 2 375 40 HSU96876 3 6 HSU96876 3 10 HSU96876 3 261 77 HSU96876 4 1015 HSU96876 4 1535 HSU96876 4 1669 HSU96876 4 1721 HSU96876 4 1738 HSU96876 4 1777 HSU96876 4 1787 HSU96876 4 2337 HSU96876 4 2844 HSU96876 4 3508 HSU96876 4 3536 HSU96876 4 3645 HSU96876 4 3715 HSU96876 4 3894 HSU96876 4 3899 HSU96876 4 3934 HSU96876 4 4169 HSU96876 4 4330 49 HUMHSP89KD 2 26 150 HUMHSP89KD 3 11 HUMHSP89KD 3 40 HUMHSP89KD 3 49 HUMHSP89KD 3 274 25 HUMHSP89KD 5 121 HUMHSP89KD 5 252 12 HUMHSP89KD 7 59 HUMHSP89KD 7 129 HUMHSP89KD 7 157 HUMHSP89KD 7 222 105 HUMHSP89KD 8 3 HUMHSP89KD 8 40 HUMHSP89KD 8 180 22 HUMHSP89KD 9 122 HUMHSP89KD 9 143 18 AF016898 1 350 AF016898 1 657 AF016898 1 1297 AF016898 1 1979 AF016898 1 2017 AF016898 1 2191 88 AF016898 2 27 AF016898 2 111 AF016898 2 115 AF016898 2 126 AF016898 2 140 AF016898 2 145 AF016898 2 245 AF016898 2 259 AF016898 2 1301 AF016898 2 1305 AF016898 2 1766 AF016898 2 1793 AF016898 2 2830 AF016898 2 3053 AF016898 2 3301 AF016898 2 4168 AF016898 2 4218 AF016898 2 4474 AF016898 2 4615 AF016898 2 5017 AF016898 2 5557 AF016898 2 5960 AF016898 2 6127 AF016898 2 6261 AF016898 2 6326 AF016898 2 7032 AF016898 2 7240 AF016898 2 8190 AF016898 2 8611 AF016898 2 8629 AF016898 2 9028 AF016898 2 9621 AF016898 2 9637 AF016898 2 9744 37 HSPEX 1 31 HSPEX 1 225 HSPEX 1 231 HSPEX 1 519 HSPEX 1 618 HSPEX 1 1160 HSPEX 1 1171 HSPEX 1 1723 HSPEX 1 3171 HSPEX 1 3758 HSPEX 1 4650 HSPEX 1 5165 66 HSPEX 2 531 HSPEX 2 778 HSPEX 2 991 HSPEX 2 1426 HSPEX 2 1497 HSPEX 2 1695 HSPEX 2 1772 HSPEX 2 2053 HSPEX 2 2113 HSPEX 2 2190 HSPEX 2 2234 HSPEX 2 2395 HSPEX 2 2404 HSPEX 2 2427 HSPEX 2 2609 HSPEX 2 2666 HSPEX 2 2833 HSPEX 2 3083 HSPEX 2 3106 HSPEX 2 3489 HSPEX 2 3526 HSPEX 2 4369 HSPEX 2 4439 HSPEX 2 4647 HSPEX 2 4795 HSPEX 2 4935 HSPEX 2 4974 HSPEX 2 5102 HSPEX 2 5224 HSPEX 2 5522 HSPEX 2 5561 HSPEX 2 5589 HSPEX 2 5683 HSPEX 2 5885 HSPEX 2 5942 HSPEX 2 6235 HSPEX 2 7044 HSPEX 2 7294 HSPEX 2 7800 HSPEX 2 7860 HSPEX 2 8130 HSPEX 2 8367 96 HSPEX 3 195 HSPEX 3 711 HSPEX 3 771 HSPEX 3 785 HSPEX 3 1139 HSPEX 3 1533 HSPEX 3 1721 HSPEX 3 1878 HSPEX 3 2137 HSPEX 3 2432 HSPEX 3 2559 HSPEX 3 2981 HSPEX 3 3153 HSPEX 3 3784 HSPEX 3 4022 HSPEX 3 4091 HSPEX 3 4105 HSPEX 3 4189 HSPEX 3 4659 HSPEX 3 4864 HSPEX 3 5251 HSPEX 3 5293 HSPEX 3 5357 HSPEX 3 5602 HSPEX 3 6189 HSPEX 3 6286 HSPEX 3 6501 HSPEX 3 7023 HSPEX 3 7158 HSPEX 3 7200 HSPEX 3 7356 HSPEX 3 7547 HSPEX 3 7624 HSPEX 3 7628 HSPEX 3 7659 HSPEX 3 7690 HSPEX 3 8230 HSPEX 3 8625 HSPEX 3 8818 HSPEX 3 8992 HSPEX 3 9084 HSPEX 3 9357 HSPEX 3 9375 HSPEX 3 9438 HSPEX 3 9748 HSPEX 3 9755 HSPEX 3 9961 HSPEX 3 10029 HSPEX 3 10160 HSPEX 3 10282 HSPEX 3 10949 HSPEX 3 11467 HSPEX 3 11870 HSPEX 3 11987 HSPEX 3 12159 HSPEX 3 12439 HSPEX 3 12512 HSPEX 3 12738 HSPEX 3 12790 HSPEX 3 12919 HSPEX 3 13247 HSPEX 3 13287 HSPEX 3 13453 HSPEX 3 13647 HSPEX 3 13651 HSPEX 3 13795 HSPEX 3 14179 HSPEX 3 14270 HSPEX 3 14350 HSPEX 3 14420 HSPEX 3 14571 HSPEX 3 14618 HSPEX 3 14666 HSPEX 3 14781 HSPEX 3 15040 HSPEX 3 15117 HSPEX 3 15141 HSPEX 3 15691 HSPEX 3 15852 HSPEX 3 15943 HSPEX 3 16159 HSPEX 3 16268 HSPEX 3 16971 HSPEX 3 16980 HSPEX 3 16984 HSPEX 3 17173 HSPEX 3 17299 HSPEX 3 17533 HSPEX 3 17697 HSPEX 3 17762 HSPEX 3 17944 HSPEX 3 18491 HSPEX 3 18662 HSPEX 3 19033 HSPEX 3 19247 HSPEX 3 19557 HSPEX 3 19575 HSPEX 3 19800 HSPEX 3 20369 HSPEX 3 20389 HSPEX 3 20443 HSPEX 3 20721 HSPEX 3 20861 HSPEX 3 20995 HSPEX 3 21455 HSPEX 3 21501 HSPEX 3 21642 HSPEX 3 21705 HSPEX 3 21821 HSPEX 3 22483 HSPEX 3 22769 HSPEX 3 22911 HSPEX 3 23377 HSPEX 3 23671 HSPEX 3 23732 HSPEX 3 24672 HSPEX 3 25102 HSPEX 3 25448 HSPEX 3 25525 HSPEX 3 25728 HSPEX 3 25839 HSPEX 3 25898 HSPEX 3 26570 HSPEX 3 26614 HSPEX 3 26768 HSPEX 3 26794 HSPEX 3 27203 HSPEX 3 27292 HSPEX 3 27434 HSPEX 3 27636 HSPEX 3 27650 HSPEX 3 28033 HSPEX 3 28119 HSPEX 3 28366 HSPEX 3 28516 HSPEX 3 28616 HSPEX 3 29136 63 HSPEX 4 539 HSPEX 4 575 HSPEX 4 823 6 HSPEX 5 1061 HSPEX 5 1112 HSPEX 5 1264 HSPEX 5 1411 HSPEX 5 1723 HSPEX 5 1946 HSPEX 5 2235 HSPEX 5 2546 HSPEX 5 3156 HSPEX 5 3882 HSPEX 5 4057 HSPEX 5 4092 HSPEX 5 4182 HSPEX 5 4442 HSPEX 5 4502 HSPEX 5 4760 HSPEX 5 4793 HSPEX 5 5082 HSPEX 5 5498 HSPEX 5 5590 HSPEX 5 5595 HSPEX 5 5898 HSPEX 5 6294 HSPEX 5 6390 HSPEX 5 6561 HSPEX 5 6684 HSPEX 5 7026 HSPEX 5 7644 HSPEX 5 7658 HSPEX 5 7775 HSPEX 5 8100 HSPEX 5 8288 HSPEX 5 8488 HSPEX 5 8680 HSPEX 5 8925 HSPEX 5 9346 HSPEX 5 10433 HSPEX 5 10612 HSPEX 5 10652 HSPEX 5 11015 HSPEX 5 11272 HSPEX 5 11279 HSPEX 5 11419 HSPEX 5 11461 HSPEX 5 11995 HSPEX 5 12579 HSPEX 5 12672 HSPEX 5 12676 4 HSPEX 6 448 41 HSPEX 6 487 HSPEX 6 964 HSPEX 6 1269 HSPEX 6 1345 HSPEX 6 1540 HSPEX 6 1975 HSPEX 6 2682 HSPEX 6 2717 HSPEX 6 2769 HSPEX 6 2802 HSPEX 6 2864 HSPEX 6 3026 HSPEX 6 3030 55 HSPEX 7 504 HSPEX 7 517 HSPEX 7 640 HSPEX 7 984 HSPEX 7 994 HSPEX 7 1020 HSPEX 7 1533 HSPEX 7 1703 HSPEX 7 1927 HSPEX 7 2083 HSPEX 7 2102 HSPEX 7 2126 HSPEX 7 2291 HSPEX 7 2304 HSPEX 7 2460 HSPEX 7 2516 13 HSPEX 8 252 HSPEX 8 430 HSPEX 8 575 HSPEX 8 681 HSPEX 8 829 HSPEX 8 996 HSPEX 8 1128 HSPEX 8 1461 HSPEX 8 1516 HSPEX 8 1629 HSPEX 8 1694 HSPEX 8 1860 136 HSPEX 9 416 HSPEX 9 1005 HSPEX 9 1009 HSPEX 9 1240 HSPEX 9 1337 HSPEX 9 1391 HSPEX 9 1430 HSPEX 9 1548 HSPEX 9 1788 HSPEX 9 2552 HSPEX 9 2871 HSPEX 9 3156 HSPEX 9 3190 HSPEX 9 3463 HSPEX 9 3508 HSPEX 9 3535 HSPEX 9 3787 HSPEX 9 3885 HSPEX 9 4223 HSPEX 9 4386 HSPEX 9 5129 HSPEX 9 5216 HSPEX 9 5307 HSPEX 9 5493 HSPEX 9 5652 HSPEX 9 5788 HSPEX 9 5846 HSPEX 9 6285 HSPEX 9 6498 HSPEX 9 6619 HSPEX 9 6651 HSPEX 9 6842 HSPEX 9 7011 HSPEX 9 7607 HSPEX 9 7886 HSPEX 9 7924 HSPEX 9 8023 HSPEX 9 8266 HSPEX 9 8273 HSPEX 9 8717 HSPEX 9 8972 HSPEX 9 9447 HSPEX 9 9576 HSPEX 9 9731 HSPEX 9 9939 HSPEX 9 10342 HSPEX 9 10466 HSPEX 9 10499 HSPEX 9 10609 HSPEX 9 10799 HSPEX 9 10851 HSPEX 9 10877 HSPEX 9 10987 HSPEX 9 11187 HSPEX 9 11227 HSPEX 9 11353 HSPEX 9 11425 HSPEX 9 11584 HSPEX 9 11628 2 HSPEX 10 187 HSPEX 10 895 HSPEX 10 902 HSPEX 10 1128 HSPEX 10 1436 HSPEX 10 1606 HSPEX 10 1611 HSPEX 10 2067 HSPEX 10 2624 HSPEX 10 2668 37 HSPEX 11 194 HSPEX 11 211 HSPEX 11 293 HSPEX 11 297 HSPEX 11 527 HSPEX 11 1088 HSPEX 11 2423 HSPEX 11 2581 HSPEX 11 3055 HSPEX 11 3169 HSPEX 11 3528 HSPEX 11 3562 HSPEX 11 3672 HSPEX 11 3784 HSPEX 11 3862 HSPEX 11 4088 HSPEX 11 5148 HSPEX 11 5289 HSPEX 11 5352 HSPEX 11 5365 HSPEX 11 5392 HSPEX 11 5651 HSPEX 11 5690 HSPEX 11 5899 HSPEX 11 6083 HSPEX 11 6250 HSPEX 11 6476 HSPEX 11 6695 HSPEX 11 6789 HSPEX 11 6816 HSPEX 11 6896 HSPEX 11 7037 HSPEX 11 7344 HSPEX 11 7509 HSPEX 11 7730 HSPEX 11 8172 HSPEX 11 8281 HSPEX 11 8544 HSPEX 11 8679 HSPEX 11 8831 HSPEX 11 9043 HSPEX 11 9124 HSPEX 11 9386 HSPEX 11 9544 HSPEX 11 9674 HSPEX 11 10415 HSPEX 11 10496 HSPEX 11 10779 HSPEX 11 10854 HSPEX 11 11312 HSPEX 11 11482 HSPEX 11 11490 HSPEX 11 11982 HSPEX 11 12091 HSPEX 11 12519 HSPEX 11 12561 HSPEX 11 12797 HSPEX 11 13141 HSPEX 11 13218 HSPEX 11 13243 HSPEX 11 13261 HSPEX 11 13353 HSPEX 11 13710 HSPEX 11 14449 HSPEX 11 14544 HSPEX 11 14555 HSPEX 11 14594 HSPEX 11 14735 HSPEX 11 15022 HSPEX 11 15675 HSPEX 11 16053 HSPEX 11 16730 HSPEX 11 17799 HSPEX 11 18181 HSPEX 11 18209 HSPEX 11 18734 139 HSPEX 12 170 HSPEX 12 281 HSPEX 12 738 HSPEX 12 752 HSPEX 12 909 HSPEX 12 1034 HSPEX 12 1104 HSPEX 12 1243 HSPEX 12 1503 HSPEX 12 1724 HSPEX 12 1818 HSPEX 12 2379 HSPEX 12 2407 HSPEX 12 2749 HSPEX 12 3112 HSPEX 12 3196 HSPEX 12 3439 HSPEX 12 3822 HSPEX 12 3854 HSPEX 12 3951 HSPEX 12 3999 HSPEX 12 4115 HSPEX 12 4819 HSPEX 12 4876 HSPEX 12 5388 HSPEX 12 5405 HSPEX 12 5679 HSPEX 12 5816 HSPEX 12 5993 HSPEX 12 6040 HSPEX 12 6288 HSPEX 12 6316 HSPEX 12 6506 HSPEX 12 6571 HSPEX 12 6620 HSPEX 12 6633 HSPEX 12 6957 HSPEX 12 7284 HSPEX 12 7288 HSPEX 12 7589 HSPEX 12 7631 HSPEX 12 8412 HSPEX 12 9038 HSPEX 12 9511 HSPEX 12 9751 HSPEX 12 9820 HSPEX 12 10313 HSPEX 12 10555 HSPEX 12 11187 HSPEX 12 11754 HSPEX 12 11772 HSPEX 12 12687 HSPEX 12 13342 HSPEX 12 13346 HSPEX 12 13496 HSPEX 12 14244 HSPEX 12 14571 HSPEX 12 14783 HSPEX 12 14855 HSPEX 12 15036 HSPEX 12 15094 HSPEX 12 15522 HSPEX 12 15556 HSPEX 12 15645 HSPEX 12 15915 HSPEX 12 16161 HSPEX 12 16217 HSPEX 12 16497 HSPEX 12 16539 HSPEX 12 17111 HSPEX 12 17137 HSPEX 12 17392 HSPEX 12 17726 HSPEX 12 17754 HSPEX 12 18520 HSPEX 12 18563 HSPEX 12 19055 HSPEX 12 19189 HSPEX 12 19355 HSPEX 12 20337 HSPEX 12 20632 HSPEX 12 20723 HSPEX 12 21037 HSPEX 12 21656 HSPEX 12 21775 HSPEX 12 21807 HSPEX 12 21893 HSPEX 12 21947 HSPEX 12 22655 HSPEX 12 22665 HSPEX 12 22701 HSPEX 12 22970 HSPEX 12 23384 HSPEX 12 23535 HSPEX 12 23635 HSPEX 12 23755 HSPEX 12 23785 HSPEX 12 23813 HSPEX 12 23922 HSPEX 12 24880 HSPEX 12 24954 HSPEX 12 25013 HSPEX 12 25201 HSPEX 12 25207 HSPEX 12 25419 HSPEX 12 25637 HSPEX 12 26163 HSPEX 12 26505 HSPEX 12 26696 HSPEX 12 26710 HSPEX 12 27147 HSPEX 12 27295 HSPEX 12 27617 HSPEX 12 28030 HSPEX 12 28517 HSPEX 12 28796 HSPEX 12 29345 HSPEX 12 30110 HSPEX 12 30207 HSPEX 12 30308 HSPEX 12 30756 HSPEX 12 30773 HSPEX 12 30876 HSPEX 12 31190 HSPEX 12 31444 HSPEX 12 31542 HSPEX 12 31651 HSPEX 12 31655 HSPEX 12 31903 HSPEX 12 32312 HSPEX 12 32963 HSPEX 12 33007 HSPEX 12 33438 HSPEX 12 33725 HSPEX 12 33993 HSPEX 12 34192 43 HSPEX 13 496 HSPEX 13 567 HSPEX 13 635 HSPEX 13 719 HSPEX 13 835 HSPEX 13 1135 HSPEX 13 1424 HSPEX 13 1742 HSPEX 13 1881 HSPEX 13 2033 HSPEX 13 2647 HSPEX 13 3292 HSPEX 13 3644 HSPEX 13 3686 HSPEX 13 3815 HSPEX 13 3892 HSPEX 13 3954 HSPEX 13 4086 HSPEX 13 4392 HSPEX 13 4507 HSPEX 13 4572 HSPEX 13 4587 HSPEX 13 4689 HSPEX 13 4850 HSPEX 13 5114 HSPEX 13 5126 HSPEX 13 5193 HSPEX 13 6451 HSPEX 13 6638 HSPEX 13 6699 HSPEX 13 6899 HSPEX 13 7061 HSPEX 13 7645 HSPEX 13 7765 HSPEX 13 8036 HSPEX 13 8324 HSPEX 13 8486 HSPEX 13 8763 HSPEX 13 8786 HSPEX 13 8790 HSPEX 13 9019 HSPEX 13 9077 HSPEX 13 9339 HSPEX 13 9606 85 HSPEX 14 40 HSPEX 14 166 HSPEX 14 382 HSPEX 14 419 HSPEX 14 589 HSPEX 14 1015 HSPEX 14 1649 HSPEX 14 1691 HSPEX 14 1806 HSPEX 14 2123 HSPEX 14 2151 HSPEX 14 2466 HSPEX 14 2731 HSPEX 14 2766 HSPEX 14 2927 HSPEX 14 3134 HSPEX 14 3438 HSPEX 14 3646 HSPEX 14 3859 HSPEX 14 4869 HSPEX 14 4966 HSPEX 14 4983 HSPEX 14 5387 HSPEX 14 6225 HSPEX 14 6315 HSPEX 14 6519 HSPEX 14 7614 HSPEX 14 7808 HSPEX 14 7891 HSPEX 14 7986 HSPEX 14 8317 HSPEX 14 8327 HSPEX 14 8919 HSPEX 14 9289 HSPEX 14 9299 HSPEX 14 9632 HSPEX 14 9646 HSPEX 14 9732 HSPEX 14 9834 HSPEX 14 10177 HSPEX 14 10252 HSPEX 14 10620 HSPEX 14 10638 HSPEX 14 11128 HSPEX 14 11146 HSPEX 14 11495 HSPEX 14 11499 HSPEX 14 11661 HSPEX 14 11823 2 HSPEX 15 73 HSPEX 15 357 HSPEX 15 398 HSPEX 15 474 HSPEX 15 480 HSPEX 15 659 HSPEX 15 1028 HSPEX 15 1174 HSPEX 15 1515 HSPEX 15 2005 HSPEX 15 2506 HSPEX 15 3110 HSPEX 15 3533 HSPEX 15 3811 HSPEX 15 3967 HSPEX 15 4056 HSPEX 15 4074 HSPEX 15 4416 HSPEX 15 4514 HSPEX 15 5341 HSPEX 15 5534 HSPEX 15 5579 HSPEX 15 6751 HSPEX 15 7033 HSPEX 15 7228 HSPEX 15 7874 HSPEX 15 7894 HSPEX 15 8041 HSPEX 15 8342 HSPEX 15 8787 HSPEX 15 9047 HSPEX 15 9218 HSPEX 15 9252 HSPEX 15 9584 HSPEX 15 9594 HSPEX 15 9680 HSPEX 15 9800 HSPEX 15 9874 HSPEX 15 10295 HSPEX 15 10311 HSPEX 15 10581 HSPEX 15 10959 HSPEX 15 11171 HSPEX 15 11330 HSPEX 15 11344 HSPEX 15 11349 HSPEX 15 11606 HSPEX 15 12554 HSPEX 15 12574 HSPEX 15 12579 HSPEX 15 12738 HSPEX 15 13502 HSPEX 15 13564 HSPEX 15 13676 HSPEX 15 13832 HSPEX 15 14103 HSPEX 15 14288 HSPEX 15 14904 HSPEX 15 15233 HSPEX 15 15754 HSPEX 15 15799 HSPEX 15 16033 HSPEX 15 16065 HSPEX 15 16173 HSPEX 15 16184 HSPEX 15 16510 HSPEX 15 16590 HSPEX 15 16736 HSPEX 15 17030 HSPEX 15 17437 HSPEX 15 17631 HSPEX 15 17702 HSPEX 15 17727 HSPEX 15 17813 HSPEX 15 18209 HSPEX 15 18249 HSPEX 15 18340 HSPEX 15 18479 HSPEX 15 18543 HSPEX 15 18572 HSPEX 15 18619 HSPEX 15 18641 HSPEX 15 18694 HSPEX 15 19369 HSPEX 15 19891 HSPEX 15 20146 HSPEX 15 20608 HSPEX 15 20652 HSPEX 15 20708 HSPEX 15 20894 HSPEX 15 20941 HSPEX 15 21025 HSPEX 15 21180 HSPEX 15 21233 HSPEX 15 21246 HSPEX 15 21505 HSPEX 15 21584 60 HSPEX 16 85 HSPEX 16 147 HSPEX 16 212 HSPEX 16 519 HSPEX 16 619 HSPEX 16 651 HSPEX 16 827 HSPEX 16 929 HSPEX 16 1038 HSPEX 16 1123 HSPEX 16 1524 HSPEX 16 2176 HSPEX 16 2204 HSPEX 16 2589 HSPEX 16 2617 HSPEX 16 3661 HSPEX 16 3796 HSPEX 16 3996 HSPEX 16 4507 HSPEX 16 4590 HSPEX 16 4685 HSPEX 16 5072 HSPEX 16 5242 HSPEX 16 5481 HSPEX 16 5558 HSPEX 16 5914 2 HSPEX 17 615 HSPEX 17 1599 HSPEX 17 2213 HSPEX 17 2437 21 HSPEX 18 291 HSPEX 18 375 HSPEX 18 760 HSPEX 18 1151 HSPEX 18 1668 HSPEX 18 1729 HSPEX 18 1769 HSPEX 18 2241 HSPEX 18 2339 HSPEX 18 2516 HSPEX 18 2541 HSPEX 18 2729 HSPEX 18 2763 HSPEX 18 2910 HSPEX 18 3074 HSPEX 18 3105 HSPEX 18 3137 HSPEX 18 3653 HSPEX 18 3912 HSPEX 18 3971 HSPEX 18 4244 HSPEX 18 4290 HSPEX 18 4337 HSPEX 18 4458 HSPEX 18 4462 HSPEX 18 4473 HSPEX 18 4579 70 HSPEX 19 133 HSPEX 19 653 HSPEX 19 842 43 HSPEX 20 138 HSPEX 20 239 HSPEX 20 508 HSPEX 20 680 HSPEX 20 805 HSPEX 20 1236 HSPEX 20 1294 HSPEX 20 2416 HSPEX 20 2887 HSPEX 20 2904 HSPEX 20 3215 HSPEX 20 3950 HSPEX 20 4172 HSPEX 20 4470 HSPEX 20 5030 HSPEX 20 5069 HSPEX 20 5087 HSPEX 20 5190 HSPEX 20 5652 HSPEX 20 6050 HSPEX 20 6277 HSPEX 20 6628 HSPEX 20 6863 HSPEX 20 7025 HSPEX 20 7501 HSPEX 20 7506 HSPEX 20 7792 HSPEX 20 7873 HSPEX 20 8415 HSPEX 20 9469 HSPEX 20 9629 HSPEX 20 10274 HSPEX 20 10278 HSPEX 20 10451 HSPEX 20 10593 HSPEX 20 10671 HSPEX 20 11150 HSPEX 20 11287 HSPEX 20 11640 HSPEX 20 11833 HSPEX 20 11886 HSPEX 20 12057 HSPEX 20 13413 HSPEX 20 13568 HSPEX 20 15246 HSPEX 20 15692 HSPEX 20 15996 HSPEX 20 16371 HSPEX 20 16771 HSPEX 20 16876 31 HSPEX 21 88 HSPEX 21 297 HSPEX 21 663 HSPEX 21 1303 HSPEX 21 1413 HSPEX 21 2129 2 HUMTNP2SS 1 14 HUMTNP2SS 1 282 HUMTNP2SS 1 421 HUMTNP2SS 1 787 9 HSU46165 1 620 HSU46165 1 696 HSU46165 1 706 54 HSU46165 2 38 HSU46165 2 104 HSU46165 3 259 HSU46165 3 299 HSU46165 3 431 HSU46165 3 587 6 HUMCP21OH 1 46 33 HUMCP21OH 2 222 45 HUMACCYBB 2 198 193 HUMACCYBB 4 34 HUMACCYBB 4 54 19 HSMGSAG 1 77 96 HSMGSAG 3 93 HSMGSAG 3 229 HSMGSAG 3 233 2 HSDAO 1 269 78 HSDAO 2 29 HSDAO 2 116 HSDAO 2 224 HSDAO 2 334 HSDAO 2 439 HSDAO 2 897 HSDAO 2 915 2 HSDAO 3 262 247 HUMATP1A2 1 37 HUMATP1A2 1 150 HUMATP1A2 1 361 HUMATP1A2 1 445 HUMATP1A2 1 663 HUMATP1A2 1 1091 HUMATP1A2 1 1280 HUMATP1A2 1 1683 HUMATP1A2 1 1688 HUMATP1A2 1 3092 HUMATP1A2 1 3237 HUMATP1A2 1 3622 HUMATP1A2 1 3630 HUMATP1A2 1 3778 HUMATP1A2 1 3899 HUMATP1A2 1 4043 HUMATP1A2 1 4307 40 HUMATP1A2 2 157 160 HUMATP1A2 3 666 HUMATP1A2 3 1259 HUMATP1A2 3 1375 HUMATP1A2 3 1648 HUMATP1A2 3 1846 HUMATP1A2 3 1903 82 HUMATP1A2 4 245 HUMATP1A2 4 367 HUMATP1A2 4 493 16 HUMATP1A2 6 205 HUMATP1A2 6 295 HUMATP1A2 6 374 HUMATP1A2 6 631 73 HUMATP1A2 7 465 HUMATP1A2 7 587 24 HUMATP1A2 8 176 HUMATP1A2 8 720 HUMATP1A2 8 767 16 HUMATP1A2 9 63 66 HUMATP1A2 10 23 148 HUMATP1A2 11 46 HUMATP1A2 11 385 HUMATP1A2 11 510 HUMATP1A2 11 617 49 HUMATP1A2 13 789 HUMATP1A2 13 805 HUMATP1A2 13 1102 HUMATP1A2 13 1269 HUMATP1A2 13 1273 HUMATP1A2 13 1303 HUMATP1A2 13 1375 HUMATP1A2 13 1967 HUMATP1A2 13 2023 HUMATP1A2 13 2458 HUMATP1A2 13 2945 112 HUMATP1A2 14 272 HUMATP1A2 14 333 HUMATP1A2 14 374 2 HUMATP1A2 19 38 16 HUMATP1A2 20 420 HUMATP1A2 20 491 HUMATP1A2 20 567 2 HUMATP1A2 22 329 150 HUMDNL1L 1 73 HUMDNL1L 1 104 HUMDNL1L 1 172 HUMDNL1L 1 179 166 HUMDNL1L 3 52 HUMDNL1L 3 57 HUMDNL1L 3 1027 2 HUMDNL1L 4 22 87 AB000381 1 296 AB000381 1 322 72 AB000381 2 321 AB000381 2 455 AB000381 2 845 AB000381 2 1130 AB000381 2 1166 AB000381 2 1460 AB000381 2 1637 AB000381 2 1770 AB000381 2 2021 AB000381 2 2406 AB000381 2 2851 AB000381 2 3118 AB000381 2 3205 AB000381 2 3224 AB000381 2 3260 AB000381 2 3820 AB000381 2 3954 AB000381 2 4370 AB000381 2 4452 AB000381 2 4528 AB000381 2 4718 AB000381 2 5225 AB000381 2 5230 213 HUMIL2RGA 1 27 30 HUMIL2RGA 2 36 HUMIL2RGA 2 104 68 HUMIL2RGA 3 103 78 HUMIL2RGA 4 15 HUMIL2RGA 4 169 HUMIL2RGA 4 307 HUMIL2RGA 4 437 HUMIL2RGA 4 503 HUMIL2RGA 4 610 HUMIL2RGA 4 685 10 HUMIL2RGA 5 280 HUMIL2RGA 5 380 HUMIL2RGA 5 391 87 HUMIL2RGA 6 94 2 HSEDMDGEN 4 287 40 HUMGASTA 1 87 12 HUMEDN1B 1 19 HUMEDN1B 1 38 HUMEDN1B 1 318 HUMEDN1B 1 469 HUMEDN1B 1 757 HUMEDN1B 1 1026 HUMEDN1B 1 1263 HUMEDN1B 1 1390 HUMEDN1B 1 1428 HUMEDN1B 1 1463 15 HUMEDN1B 2 336 HUMEDN1B 2 343 HUMEDN1B 2 347 HUMEDN1B 2 479 HUMEDN1B 2 780 HUMEDN1B 2 1018 HUMEDN1B 2 1358 2 HUMEDN1B 4 24 HUMEDN1B 4 102 HUMEDN1B 4 250 HUMEDN1B 4 601 HUMEDN1B 4 1516 2 HSTPI1G 1 172 HSTPI1G 1 225 HSTPI1G 1 811 HSTPI1G 1 874 HSTPI1G 1 938 HSTPI1G 1 1070 228 HSTPI1G 2 20 2 HSTPI1G 4 165 24 HSTPI1G 6 67 45 AC002482 1 499 AC002482 1 752 96 HSHHA2GEN 1 11 HSHHA2GEN 1 16 HSHHA2GEN 1 356 19 HSHHA2GEN 3 401 HSHHA2GEN 3 1013 HSHHA2GEN 3 1109 HSHHA2GEN 3 1273 160 HSHHA2GEN 5 201 HSHHA2GEN 5 337 HSHHA2GEN 5 455 HSHHA2GEN 5 589 HSHHA2GEN 5 902 49 HSHHA2GEN 6 335 HSHHA2GEN 6 596 HSHHA2GEN 6 854 HSHHA2GEN 6 1112 HSHHA2GEN 6 1533 HSHHA2GEN 6 1546 HSHHA2GEN 6 1551 HSHHA2GEN 6 1680 HSHHA2GEN 6 1741 HSHHA2GEN 6 1745 HSHHA2GEN 6 1839 HSHHA2GEN 6 1879 HSHHA2GEN 6 1897 HSHHA2GEN 6 1995 HSHHA2GEN 6 2055 HSHHA2GEN 6 2425 23 HSINSU 1 577 126 AF000573 1 178 AF000573 1 486 AF000573 1 629 AF000573 1 663 AF000573 1 968 AF000573 1 1241 AF000573 1 1270 AF000573 1 1451 AF000573 1 1575 AF000573 1 1726 AF000573 1 1890 AF000573 1 1954 AF000573 1 2131 AF000573 1 2219 AF000573 1 2570 AF000573 1 2696 AF000573 1 2801 AF000573 1 4000 AF000573 1 4225 AF000573 1 4575 AF000573 1 4686 AF000573 1 4770 AF000573 1 4802 AF000573 1 4835 AF000573 1 5957 AF000573 1 5977 94 AF000573 2 297 AF000573 2 322 AF000573 2 492 AF000573 2 546 AF000573 2 750 4 AF000573 3 174 AF000573 3 191 AF000573 3 411 AF000573 3 591 AF000573 3 666 AF000573 3 720 AF000573 3 843 AF000573 3 965 AF000573 3 1045 AF000573 3 1066 AF000573 3 1114 AF000573 3 1261 AF000573 3 1408 AF000573 3 1720 AF000573 3 2163 AF000573 3 2223 AF000573 3 2405 AF000573 3 2789 AF000573 3 2802 AF000573 3 3475 AF000573 3 3640 AF000573 3 4060 AF000573 3 4171 11 AF000573 4 127 AF000573 4 205 AF000573 4 457 AF000573 4 496 AF000573 4 521 AF000573 4 1066 AF000573 4 1094 AF000573 4 1122 AF000573 4 1246 AF000573 4 1568 AF000573 4 1715 AF000573 4 1810 AF000573 4 2176 AF000573 4 2845 AF000573 4 3218 AF000573 4 3473 AF000573 4 3706 AF000573 4 3776 AF000573 4 3859 AF000573 4 4552 AF000573 4 5145 AF000573 4 5624 AF000573 4 5874 AF000573 4 5900 AF000573 4 5912 AF000573 4 6981 AF000573 4 7041 AF000573 4 7878 AF000573 4 7966 AF000573 4 8628 AF000573 4 9117 AF000573 4 9149 AF000573 4 9276 AF000573 4 9482 AF000573 4 9809 AF000573 4 10039 AF000573 4 10190 AF000573 4 10310 AF000573 4 10419 AF000573 4 10737 AF000573 4 11031 AF000573 4 11828 AF000573 4 12151 AF000573 4 12295 AF000573 4 12400 AF000573 4 12417 AF000573 4 12488 AF000573 4 12492 AF000573 4 12523 AF000573 4 12609 AF000573 4 12766 AF000573 4 12784 AF000573 4 13144 AF000573 4 13627 AF000573 4 14013 AF000573 4 14406 AF000573 4 14557 AF000573 4 14848 AF000573 4 15027 AF000573 4 15073 AF000573 4 15381 AF000573 4 15465 AF000573 4 15629 AF000573 4 15821 AF000573 4 16019 AF000573 4 16240 AF000573 4 16331 AF000573 4 16409 AF000573 4 17484 AF000573 4 17612 AF000573 4 17659 46 AF000573 5 3 AF000573 5 48 AF000573 5 527 AF000573 5 667 AF000573 5 1471 AF000573 5 1532 55 AF000573 6 422 AF000573 6 1390 AF000573 6 1406 AF000573 6 2090 AF000573 6 2124 AF000573 6 2804 2 AF000573 7 296 AF000573 7 526 9 AF000573 9 412 AF000573 9 455 AF000573 9 952 AF000573 9 1277 60 AF000573 10 210 AF000573 10 303 AF000573 10 364 AF000573 10 702 AF000573 10 962 AF000573 10 1386 AF000573 10 1726 AF000573 10 2434 AF000573 10 2453 7 AF000573 11 138 AF000573 11 833 AF000573 11 1789 AF000573 11 1826 AF000573 11 2948 31 AF000573 12 1132 AF000573 12 1286 AF000573 12 1385 AF000573 12 1822 AF000573 12 1936 AF000573 12 2254 AF000573 12 2503 AF000573 12 2669 AF000573 12 2701 AF000573 12 2746 AF000573 12 2817 AF000573 12 3371 AF000573 12 3602 AF000573 12 3660 AF000573 12 3957 AF000573 12 4100 AF000573 12 4279 AF000573 12 4326 75 AF000573 13 3 AF000573 13 128 AF000573 13 386 AF000573 13 767 AF000573 13 1602 AF000573 13 1666 AF000573 13 1959 AF000573 13 2142 AF000573 13 2309 AF000573 13 2673 AF000573 13 3101 AF000573 13 3408 AF000573 13 3503 AF000573 13 3749 AF000573 13 3826 AF000573 13 4249 AF000573 13 4356 127 HUMGCB1 2 3 HUMGCB1 2 140 HUMGCB1 2 274 HUMGCB1 2 383 HUMGCB1 2 425 HUMGCB1 2 452 6 HUMGCB1 3 48 45 HUMGCB1 4 480 HUMGCB1 4 522 27 HUMGCB1 5 62 136 HUMGCB1 6 482 2 HUMGCB1 7 181 HUMGCB1 7 238 HUMGCB1 7 324 HUMGCB1 7 399 HUMGCB1 7 503 HUMGCB1 7 507 HUMGCB1 7 676 103 HUMGCB1 9 155 HUMGCB1 9 217 HUMGCB1 9 283 HUMGCB1 9 295 HUMGCB1 9 299 2 HUMGCB1 10 11 2 HUMATPSYB 1 222 HUMATPSYB 1 232 81 HUMATPSYB 3 64 HUMATPSYB 3 252 HUMATPSYB 3 294 HUMATPSYB 3 387 HUMATPSYB 3 538 HUMATPSYB 3 687 HUMATPSYB 3 701 HUMATPSYB 3 721 HUMATPSYB 3 786 2 HUMATPSYB 7 132 HUMATPSYB 7 212 HUMATPSYB 7 227 HUMATPSYB 7 671 HUMATPSYB 7 838 HUMATPSYB 7 1173 HUMATPSYB 7 1274 HUMATPSYB 7 1308 HUMATPSYB 7 1837 HUMATPSYB 7 1889 HUMATPSYB 7 1991 16 HUMATPSYB 8 334 HUMATPSYB 8 468 HUMATPSYB 8 598 127 HUMATPSYB 9 295 HUMATPSYB 9 431 HUMATPSYB 9 607 75 HSPSAG 1 424 603 HSPSAG 2 29 HSPSAG 2 235 HSPSAG 2 534 HSPSAG 2 548 HSPSAG 2 830 2 HSPSAG 3 101 48 HSPSAG 4 35 HSPSAG 4 178 HSPSAG 4 382 HSPSAG 4 448 HSPSAG 4 1006 109 HUMEF1A 1 61 HUMEF1A 1 79 HUMEF1A 1 142 HUMEF1A 1 166 64 HUMEF1A 4 58 57 HUMPSAP 1 138 105 HUMPSAP 2 17 HUMPSAP 2 52 HUMPSAP 2 123 HUMPSAP 2 157 HUMPSAP 2 195 HUMPSAP 2 248 HUMPSAP 2 322 HUMPSAP 2 401 126 HUMPSAP 3 272 HUMPSAP 3 287 HUMPSAP 3 317 HUMPSAP 3 412 HUMPSAP 3 421 HUMPSAP 3 440 78 HSFESFPS 1 20 HSFESFPS 2 96 HSFESFPS 2 335 313 HSFESFPS 4 308 HSFESFPS 4 389 HSFESFPS 4 432 HSFESFPS 4 536 HSFESFPS 4 671 HSFESFPS 4 835 HSFESFPS 4 1185 HSFESFPS 4 1210 HSFESFPS 4 1817 2 HSFESFPS 9 456 HSFESFPS 9 464 46 HSFESFPS 10 179 82 HSFESFPS 11 122 HSFESFPS 11 201 76 HSFESFPS 12 476 97 HSFESFPS 14 24 27 HSFESFPS 15 52 2 HSFESFPS 17 298 HSFESFPS 17 429 HSFESFPS 17 610 HSFESFPS 17 780 243 HUNPIV 1 92 HUNPIV 1 160 HUNPIV 1 197 HUNPIV 1 350 141 HUMIMPDH 2 34 37 HUMIMPDH 4 48 46 HUMIMPDH 5 222 HUMIMPDH 5 482 46 HUMIMPDH 7 16 57 HUMIMPDH 8 41 HUMIMPDH 9 328 HUMIMPDH 9 744 HUMIMPDH 9 854 HUMIMPDH 9 864 15 HSU73002 1 234 HSU73002 1 378 237 HSU73002 2 117 HSU73002 2 267 87 HSU73002 3 415 HSU73002 3 432 25 HSU73002 4 431 25 HUMHIAPPA 1 587 HUMHIAPPA 1 682 HUMHIAPPA 1 738 HUMHIAPPA 1 1046 HUMHIAPPA 1 1485 HUMHIAPPA 1 1787 HUMHIAPPA 1 2162 HUMHIAPPA 1 2398 HUMHIAPPA 1 2412 HUMHIAPPA 1 2502 HUMHIAPPA 1 2701 HUMHIAPPA 1 2936 HUMHIAPPA 1 3327 HUMHIAPPA 1 3708 HUMHIAPPA 1 3879 HUMHIAPPA 1 4117 HUMHIAPPA 1 4507 HUMHIAPPA 1 4665 47 HSU32323 2 163 HSU32323 2 237 HSU32323 2 333 HSU32323 2 735 HSU32323 2 815 HSU32323 2 880 2 HSU32323 3 59 87 HSU32323 4 52 HSU32323 4 73 83 HSU32323 5 6 2 HSU32323 6 431 99 HSU32323 7 140 HSU32323 7 147 HSU32323 7 192 HSU32323 7 349 HSU32323 7 747 HSU32323 7 1033 46 HSU32323 8 80 HSU32323 8 274 57 HSU32323 10 3 2 HSU32323 11 316 6 HUMG0S19A 1 187 HUMG0S19A 1 305 HUMG0S19A 1 465 75 HUMG0S19A 2 33 HUMG0S19A 2 134 2 HUMPGAMMG 2 27 HUMPGAMMG 2 224 HUMPGAMMG 2 992 HUMPGAMMG 2 1307 HUMPGAMMG 2 1560 126 HUMCYPBB 2 71 HUMCYPBB 2 121 HUMCYPBB 2 327 HUMCYPBB 2 489 HUMCYPBB 2 501 HUMCYPBB 2 541 HUMCYPBB 2 606 HUMCYPBB 2 754 HUMCYPBB 2 978 HUMCYPBB 2 987 HUMCYPBB 2 1425 HUMCYPBB 2 1430 HUMCYPBB 2 1511 2 HUMCYPBB 5 179 HUMCYPBB 5 535 34 HUMCYPBB 8 173 HUMCYPBB 8 288 151 HUMTSHB2 1 156 HUMTSHB2 1 364 31 HSIL1RECA 1 24 HSIL1RECA 1 240 HSIL1RECA 1 673 HSIL1RECA 1 855 HSIL1RECA 1 996 HSIL1RECA 1 1023 HSIL1RECA 1 1031 HSIL1RECA 1 1049 HSIL1RECA 1 1153 HSIL1RECA 1 1351 HSIL1RECA 1 1439 HSIL1RECA 1 1456 HSIL1RECA 1 1592 2 HSIL1RECA 2 208 HSIL1RECA 2 215 HSIL1RECA 2 872 HSIL1RECA 2 958 HSIL1RECA 2 1044 HSIL1RECA 2 1130 90 HSIL1RECA 3 707 HSIL1RECA 3 764 HSIL1RECA 3 952 HSIL1RECA 3 1059 HSIL1RECA 3 1075 HSIL1RECA 3 1149 94 HUMIL8A 1 249 HUMIL8A 1 257 HUMIL8A 1 326 57 HUMIL8A 3 100 HUMIL8A 3 142 2 HSS100A2 1 33 HSS100A2 1 288 HSS100A2 1 601 HSS100A2 1 674 HSS100A2 1 1002 HSS100A2 1 1053 HSS100A2 1 1161 HSS100A2 1 1478 HSS100A2 1 1516 55 HUMGFP40H 3 404 HUMGFP40H 3 574 HUMGFP40H 3 672 HUMGFP40H 3 769 HUMGFP40H 3 1187 16 HUMGFP40H 4 34 HUMGFP40H 4 45 HUMGFP40H 4 158 HUMGFP40H 4 187 HUMGFP40H 4 490 HUMGFP40H 4 532 HUMGFP40H 4 625 HUMGFP40H 4 667 HUMGFP40H 4 701 HUMGFP40H 4 832 HUMGFP40H 4 1239 HUMGFP40H 4 1431 37 HSUBR 1 310 HSUBR 1 333 2 HUMBLYM1 1 96 8 HSCYP450 1 20 HSCYP450 1 65 HSCYP450 1 505 124 HSCYP450 3 24 6 HSCYP450 4 64 2 HSZNGP1 1 46 HSZNGP1 1 623 HSZNGP1 1 788 HSZNGP1 1 2153 HSZNGP1 1 2751 HSZNGP1 1 3214 HSZNGP1 1 3482 HSZNGP1 1 3679 276 HSZNGP1 2 58 HSZNGP1 2 1033 HSZNGP1 2 1086 HSZNGP1 2 1271 HSZNGP1 2 1628 HSZNGP1 2 1683 HSZNGP1 2 1716 HSZNGP1 2 1946 HSZNGP1 2 2556 HSZNGP1 2 2691 6 HSZNGP1 3 274 HSZNGP1 3 283 HSZNGP1 3 672 HSZNGP1 3 677 78 HSU09954 2 40 HSU09954 2 289 HSU09954 2 373 HSU09954 2 436 HSU09954 2 444 196 HSU09954 3 66 HSU09954 3 512 HSU09954 3 762 HSU09954 3 916 HSU09954 3 942 112 HSU09954 4 295 HSU09954 4 307 HSU09954 4 412 HSU09954 4 718 HSU09954 4 760 HSU09954 4 1315 HSU09954 4 1389 114 HUMTFPB 1 323 HUMTFPB 1 964 HUMTFPB 1 1065 HUMTFPB 1 1087 HUMTFPB 1 1095 156 HUMTFPB 2 394 HUMTFPB 2 817 HUMTFPB 2 905 HUMTFPB 2 1104 HUMTFPB 2 1108 HUMTFPB 2 1284 HUMTFPB 2 1468 HUMTFPB 2 1569 HUMTFPB 2 1599 HUMTFPB 2 1663 HUMTFPB 2 2830 HUMTFPB 2 2968 HUMTFPB 2 3830 2 HUMTFPB 3 119 HUMTFPB 3 207 HUMTFPB 3 267 HUMTFPB 3 788 HUMTFPB 3 827 HUMTFPB 3 922 HUMTFPB 3 977 HUMTFPB 3 1040 HUMTFPB 3 1750 HUMTFPB 3 1867 HUMTFPB 3 2456 18 HUMTFPB 4 108 13 HUMTFPB 5 45 HUMTFPB 5 235 HUMTFPB 5 407 HUMTFPB 5 503 HUMTFPB 5 522 HUMTFPB 5 787 HUMTFPB 5 942 HUMTFPB 5 1579 48 HSCD1R3 1 91 21 HSCD1R3 2 186 117 HSCD1R3 3 123 HSCD1R3 3 390 126 HSCD1R3 4 93 HSCD1R3 4 325 114 HSU96846 1 60 HSU96846 1 303 36 HSU96846 2 462 24 HSU96846 3 27 HSU96846 3 384 54 HSL7A 1 140 HSL7A 1 502 13 HSL7A 2 53 HSL7A 2 343 6 HSL7A 3 200 123 HSL7A 4 170 159 HSL7A 5 72 HSL7A 5 90 HSL7A 5 94 HSL7A 5 145 22 HSL7A 6 208 2 HSUSF2 5 25 9 HSUSF2 7 10 HSUSF2 7 148 HSUSF2 7 400 HSUSF2 7 404 HSUSF2 7 515 HSUSF2 7 808 HSUSF2 7 955 HSUSF2 7 1230 HSUSF2 7 1351 HSUSF2 7 1561 HSUSF2 7 1713 HSUSF2 7 1856 HSUSF2 7 2320 HSUSF2 7 2370 HSUSF2 7 2578 HSUSF2 7 2739 HSUSF2 7 2782 HSUSF2 7 3220 HSUSF2 7 3362 HSUSF2 7 4006 HSUSF2 7 4284 HSUSF2 7 4725 HSUSF2 7 4759 HSUSF2 7 4768 HSUSF2 7 5688 HSUSF2 7 5803 HSUSF2 7 5814 HSUSF2 7 6328 HSUSF2 7 6921 138 HSFAU1 2 32 HSFAU1 2 43 HSFAU1 2 252 6 HSFAU1 3 127 157 HSCSRP2S2 1 512 HSCSRP2S2 1 683 HSCSRP2S2 1 1531 HSCSRP2S2 1 1580 HSCSRP2S2 1 1907 HSCSRP2S2 1 2235 HSCSRP2S2 1 2596 HSCSRP2S2 1 2675 6 HSCSRP2S2 2 255 HSCSRP2S2 2 347 HSCSRP2S2 2 365 HSCSRP2S2 2 717 HSCSRP2S2 2 1417 HSCSRP2S2 2 1732 HSCSRP2S2 2 1736 HSCSRP2S2 2 2381 HSCSRP2S2 2 2426 2 HSCSRP2S2 3 161 HSCSRP2S2 3 270 235 HSCSRP2S2 4 239 111 D49493 1 102 D49493 1 768 D49493 1 791 D49493 1 829 D49493 1 915 D49493 1 987 D49493 1 1079 D49493 1 1220 D49493 1 1517 D49493 1 1752 D49493 1 1948 D49493 1 1966 D49493 1 2014 D49493 1 2178 D49493 1 2281 D49493 1 2357 D49493 1 2588 D49493 1 2666 D49493 1 2734 D49493 1 2765 D49493 1 2777 D49493 1 2992 D49493 1 3158 D49493 1 3173 D49493 1 3681 D49493 1 3725 D49493 1 3775 D49493 1 3788 D49493 1 3998 D49493 1 4193 D49493 1 4217 D49493 1 4875 D49493 1 5555 D49493 1 5932 D49493 1 5950 D49493 1 5961 D49493 1 7386 D49493 1 7409 D49493 1 7629 D49493 1 8670 D49493 1 8735 6 D49493 2 194 D49493 2 766 D49493 2 915 D49493 2 1216 D49493 2 1239 D49493 2 1314 D49493 2 1745 D49493 2 1821 D49493 2 1829 D49493 2 1833 D49493 2 1850 31 HSU01882 1 20 133 HSU01882 2 291 HSU01882 2 501 HSU01882 2 581 HSU01882 2 588 HSU01882 2 742 HSU01882 2 752 HSU01882 2 809 HSU01882 2 994 16 HSU01882 3 366 HSU01882 3 657 43 HSU01882 4 62 HSU01882 4 183 HSU01882 4 401 HSU01882 4 459 2 HSU01882 5 93 HSU01882 5 120 HSU01882 5 144 123 HSU96402 2 172 175 HSACKI10 1 6 HSACKI10 1 510 HSACKI10 1 512 HSACKI10 1 692 64 HSACKI10 2 146 HSACKI10 2 195 2 HSACKI10 5 95 7 HSU78190 1 228 HSU78190 1 232 HSU78190 1 579 HSU78190 1 770 HSU78190 1 933 376 HSU78190 2 567 HSU78190 2 1198 2 HUMCOX5B 1 443 375 HUMCOX5B 2 127 55 HUMCOX5B 3 80 HUMCOX5B 3 94 HUMCOX5B 3 178 HUMCOX5B 3 358 HUMCOX5B 3 374 36 HSHCF1 2 33 2 HSHCF1 3 83 HSHCF1 3 88 HSHCF1 3 592 210 HSHCF1 4 343 HSHCF1 4 385 2 HSHCF1 5 290 HSHCF1 5 504 HSHCF1 5 857 HSHCF1 5 889 HSHCF1 5 1076 183 HSHCF1 7 275 39 HSHCF1 8 175 HSHCF1 8 374 HSHCF1 8 494 HSHCF1 8 516 67 HSHCF1 9 120 HSHCF1 9 212 88 HSHCF1 10 39 136 HSHCF1 15 54 HSHCF1 15 249 HSHCF1 15 456 HSHCF1 15 477 HSHCF1 15 516 13 HSHCF1 17 290 HSHCF1 17 431 127 HSHCF1 18 322 153 HSHCF1 19 50 HSHCF1 20 8 25 HSHCF1 21 29 HSHCF1 21 33 HSHCF1 21 122 19 HSHCF1 23 299 HSHCF1 23 388 HSHCF1 23 433 HSHCF1 23 475 213 HSU25826 1 544 HSU25826 1 776 HSU25826 1 832 HSU25826 1 909 HSU25826 1 1094 HSU25826 1 1234 HSU25826 1 1610 9 HSU25826 2 180 2 HSRAS1 2 40 2 HSRAS1 3 175 112 Accession Intron Latents First No. No. Pos. Stop codon Pos. D83657 1 3 46 HSGROW2 1 116 12 HSGROW2 2 44 82 HUMI309 1 153 HUMI309 1 263 HUMI309 1 745 HUMI309 1 1030 HUMI309 1 1137 120 HUMI309 2 176 HUMI309 2 378 HUMI309 2 575 HUMI309 2 763 2 HSPAT133 1 218 HSPAT133 1 334 333 HSU20758 2 129 HSU20758 2 189 HSU20758 2 205 25 HSU20758 4 194 46 HSU20758 5 172 37 HSU82827 1 77 HSU82827 1 196 HSU82827 1 280 HSU82827 1 430 HSU82827 1 520 6 HSU17969 1 340 HSU17969 1 429 HSU17969 1 950 HSU17969 1 1113 HSU17969 1 1141 94 HUMCYP2DG 1 66 HUMCYP2DG 1 479 HUMCYP2DG 1 540 73 HUMCYP2DG 2 32 HUMCYP2DG 2 140 HUMCYP2DG 2 217 HUMCYP2DG 2 361 HUMCYP2DG 2 395 287 HUMCYP2DG 4 180 HUMCYP2DG 4 312 HUMCYP2DG 4 317 HUMCYP2DG 4 324 HUMCYP2DG 4 383 91 HUMCYP2DG 5 33 HUMCYP2DG 5 136 118 HUMCYP2DG 7 71 HUMCYP2DG 7 277 46 HUMPRCA 1 102 HUMPRCA 1 107 HUMPRCA 1 152 HUMPRCA 1 718 HUMPRCA 1 979 HUMPRCA 1 1236 105 HUMPRCA 2 71 HUMPRCA 2 164 HUMPRCA 2 224 HUMPRCA 2 251 HUMPRCA 2 363 HUMPRCA 2 543 HUMPRCA 2 1146 88 HUMPRCA 4 12 HUMPRCA 5 1018 HUMPRCA 5 1191 HUMPRCA 5 1666 HUMPRCA 5 1832 HUMPRCA 5 2236 HUMPRCA 5 2408 60 HUMPRCA 6 127 HUMPRCA 6 183 HUMPRCA 6 187 HUMPRCA 6 645 121 HUMPRCA 7 91 HUMPRCA 7 127 HUMPRCA 7 232 HUMPRCA 7 667 HUMPRCA 7 961 45 AF041427 1 100 AF041427 1 200 AF041427 1 345 25 AF041427 2 259 AF041427 2 713 AF041427 2 1085 AF041427 2 1202 AF041427 2 1440 AF041427 2 1757 43 AF041427 3 205 AF041427 3 659 AF041427 3 669 AF041427 3 778 AF041427 3 1033 AF041427 3 1083 399 AF041427 4 17 AF041427 4 45 AF041427 4 137 AF041427 4 203 AF041427 4 404 AF041427 4 652 AF041427 4 722 AF041427 4 726 AF041427 4 924 AF041427 4 1295 AF041427 4 1455 AF041427 4 1520 AF041427 4 1708 AF041427 4 1722 AF041427 4 1765 AF041427 4 1825 AF041427 4 1933 AF041427 4 2086 AF041427 4 2203 AF041427 4 2400 AF041427 4 2892 AF041427 4 3055 AF041427 4 3090 AF041427 4 3783 AF041427 4 3836 AF041427 4 3937 AF041427 4 4081 AF041427 4 4089 AF041427 4 4108 AF041427 4 4114 AF041427 4 4222 AF041427 4 4243 AF041427 4 4596 AF041427 4 4777 AF041427 4 4789 AF041427 4 4926 AF041427 4 5465 AF041427 4 5489 AF041427 4 5538 AF041427 4 5893 AF041427 4 6026 AF041427 4 6656 AF041427 4 6854 AF041427 4 6913 AF041427 4 7753 AF041427 4 7946 AF041427 4 8218 AF041427 4 8321 AF041427 4 8589 AF041427 4 8791 76 AF041427 5 191 AF041427 5 336 AF041427 5 549 AF041427 5 1253 AF041427 5 1310 AF041427 5 1314 AF041427 5 1493 AF041427 5 1509 AF041427 5 1924 AF041427 5 2005 AF041427 5 2047 AF041427 5 2878 AF041427 5 2985 AF041427 5 3058 AF041427 5 3327 AF041427 5 3331 AF041427 5 3517 AF041427 5 3752 AF041427 5 3815 AF041427 5 3992 AF041427 5 4005 AF041427 5 4478 AF041427 5 4918 AF041427 5 6547 AF041427 5 7077 AF041427 5 7215 AF041427 5 7424 AF041427 5 7757 AF041427 5 7771 AF041427 5 8070 AF041427 5 8120 AF041427 5 8758 AF041427 5 8850 AF041427 5 9037 AF041427 5 9063 AF041427 5 9517 AF041427 5 9579 AF041427 5 10225 102 AF041427 6 292 AF041427 6 335 AF041427 6 339 AF041427 6 426 AF041427 6 1155 AF041427 6 1237 AF041427 6 1459 AF041427 6 1470 106 HUMG0S8PP 1 130 HUMG0S8PP 1 143 HUMG0S8PP 1 353 HUMG0S8PP 1 487 HUMG0S8PP 1 832 HUMG0S8PP 1 894 2 HUMG0S8PP 2 67 2 HUMG0S8PP 3 180 HUMG0S8PP 3 466 66 HUMMIS 1 45 HUMMIS 1 154 63 HUMMIS 2 130 85 HSU49742 1 1051 HSU49742 1 1088 HSU49742 1 1189 84 HSU49742 2 480 HSU49742 2 1029 2 HSU49742 4 228 HSU49742 4 249 HSU49742 4 403 HSU49742 4 659 442 HSPXFGEN 1 275 HSPXFGEN 1 688 HSPXFGEN 1 716 HSPXFGEN 1 793 HSPXFGEN 1 917 HSPXFGEN 1 1016 HSPXFGEN 1 1222 HSPXFGEN 1 1268 12 HSPXFGEN 2 116 HSPXFGEN 2 321 HSPXFGEN 2 383 4 HSPXFGEN 3 164 120 HSPXFGEN 4 161 13 HSPXFGEN 5 190 HSPXFGEN 5 404 HSPXFGEN 5 854 HSPXFGEN 5 1078 HSPXFGEN 5 1082 HSPXFGEN 5 1086 HSPXFGEN 5 1181 HSPXFGEN 5 1402 HSPXFGEN 5 1442 HSPXFGEN 5 1624 52 HSPXFGEN 7 80 28 HUMVIPAA 1 138 HUMVIPAA 1 322 HUMVIPAA 1 498 HUMVIPAA 1 776 HUMVIPAA 1 1119 HUMVIPAA 1 1357 HUMVIPAA 1 1437 2 HUMVIPAA 2 449 HUMVIPAA 2 472 HUMVIPAA 2 808 2 HUMVIPAA 3 306 HUMVIPAA 3 429 HUMVIPAA 3 700 2 HUMVIPAA 4 445 HUMVIPAA 4 489 2 HUMOP18A 1 3 6 HUMOP18A 2 277 HUMOP18A 2 498 HUMOP18A 2 643 HUMOP18A 2 749 HUMOP18A 2 763 HUMOP18A 2 768 HUMOP18A 2 872 HUMOP18A 2 1074 HUMOP18A 2 1132 HUMOP18A 2 1142 HUMOP18A 2 1426 HUMOP18A 2 1740 HUMOP18A 2 1800 151 HUMOP18A 3 82 HUMOP18A 3 135 HUMOP18A 3 320 40 HSCBMYHC 1 16 19 HSCBMYHC 7 123 HSCBMYHC 7 207 48 HSCBMYHC 9 167 HSCBMYHC 9 326 HSCBMYHC 9 344 HSCBMYHC 9 390 HSCBMYHC 9 394 10 HSCBMYHC 10 181 HSCBMYHC 10 292 93 HSCBMYHC 13 358 55 HSCBMYHC 14 63 57 HSCBMYHC 17 73 HSCBMYHC 17 121 8 HSCBMYHC 18 207 16 HSCBMYHC 19 207 2 HSCBMYHC 22 552 HSCBMYHC 22 844 HSCBMYHC 22 1111 202 HSCBMYHC 23 175 HSCBMYHC 23 764 44 HSCBMYHC 24 163 202 HSCBMYHC 26 143 165 HSCBMYHC 28 206 2 HSCBMYHC 29 86 157 HSCBMYHC 32 86 HSCBMYHC 32 109 85 HSCBMYHC 34 60 67 HSCBMYHC 35 11 HSCBMYHC 35 168 HSCBMYHC 35 398 HSCBMYHC 35 496 HSCBMYHC 35 734 40 HSCBMYHC 37 128 25 HUMIBP3 1 15 HUMIBP3 1 142 HUMIBP3 1 403 HUMIBP3 1 493 HUMIBP3 1 569 HUMIBP3 1 700 HUMIBP3 1 707 HUMIBP3 1 914 HUMIBP3 1 1482 HUMIBP3 1 1511 HUMIBP3 1 1542 HUMIBP3 1 1805 HUMIBP3 1 1862 HUMIBP3 1 1916 HUMIBP3 1 1964 HUMIBP3 1 2034 HUMIBP3 1 2482 HUMIBP3 1 2680 HUMIBP3 1 3111 HUMIBP3 1 3144 264 HUMIBP3 2 421 106 HUMIBP3 3 146 HUMIBP3 3 519 HUMIBP3 3 566 HUMIBP3 3 631 HUMIBP3 3 759 HUMIBP3 3 1069 HUMIBP3 3 1224 HUMIBP3 3 1307 88 S45332 1 178 S45332 1 627 72 S45332 2 248 S45332 2 652 S45332 2 777 2 S45332 6 381 S45332 6 408 S45332 6 742 S45332 6 829 S45332 6 1104 S45332 6 1198 S45332 6 1202 S45332 6 1236 S45332 6 1388 S45332 6 1516 S45332 6 1619 S45332 6 1870 S45332 6 2048 S45332 6 2074 2 S45332 7 75 70 HUMMRP14A 1 245 HUMMRP14A 1 390 HUMMRP14A 1 430 HUMMRP14A 1 811 HUMMRP14A 1 851 HUMMRP14A 1 1147 HUMMRP14A 1 1243 HUMMRP14A 1 1563 HUMMRP14A 1 1690 301 L29472 1 70 L29472 1 145 L29472 1 497 L29472 1 579 L29472 1 606 L29472 1 675 L29472 1 953 L29472 1 999 L29472 1 1295 L29472 1 1475 207 L29472 3 321 9 L29472 5 147 25 HUMIRBPG 1 39 HUMIRBPG 1 218 HUMIRBPG 1 368 HUMIRBPG 1 679 HUMIRBPG 1 1139 HUMIRBPG 1 1366 HUMIRBPG 1 1417 HUMIRBPG 1 1430 HUMIRBPG 1 1490 HUMIRBPG 1 1504 HUMIRBPG 1 1554 HUMIRBPG 1 1678 88 HUMIRBPG 2 13 HUMIRBPG 2 182 HUMIRBPG 2 398 HUMIRBPG 2 410 HUMIRBPG 2 417 HUMIRBPG 2 687 HUMIRBPG 2 917 HUMIRBPG 2 1179 HUMIRBPG 2 1434 344 HUMIRBPG 3 77 HUMIRBPG 3 100 HUMIRBPG 3 268 HUMIRBPG 3 787 HUMIRBPG 3 1279 153 HSMED 1 237 HSMED 1 419 147 HSMED 2 54 2 HSMED 3 838 HSMED 3 1583 HSMED 3 2039 427 HSMED 4 116 79 HSU57623 1 141 HSU57623 1 253 HSU57623 1 264 HSU57623 1 491 HSU57623 1 868 HSU57623 1 1454 HSU57623 1 1917 HSU57623 1 2077 93 HSU57623 2 176 HSU57623 2 314 HSU57623 2 432 HSU57623 2 851 HSU57623 2 909 HSU57623 2 1067 HSU57623 2 1253 HSU57623 2 1713 46 HSU57623 3 141 HSU57623 3 884 HSU57623 3 946 HSU57623 3 1283 HSU57623 3 1337 160 HSU10307 1 42 HSU10307 1 46 HSU10307 1 102 HSU10307 1 197 HSU10307 1 531 HSU10307 1 555 13 HSU10307 3 88 211 HUMPRPH1 1 711 HUMPRPH1 1 727 HUMPRPH1 1 1015 27 HUMPRPH1 2 260 HUMPRPH1 2 301 12 AC002132 1 55 9 AC002132 2 325 AC002132 2 3166 AC002132 2 3500 120 AC002132 4 294 AC002132 4 467 AC002132 4 515 AC002132 4 1396 AC002132 4 1438 AC002132 4 1811 108 AC002132 5 880 AC002132 5 1408 AC002132 5 2108 AC002132 5 2174 AC002132 5 2248 AC002132 5 2739 AC002132 5 4006 AC002132 5 4087 AC002132 5 4249 AC002132 5 4643 AC002132 5 4648 AC002132 5 4652 AC002132 5 4678 AC002132 5 4682 AC002132 5 4692 AC002132 5 5091 AC002132 5 5146 AC002132 5 5391 AC002132 5 5395 AC002132 5 5413 AC002132 5 6043 AC002132 5 6296 AC002132 5 6365 AC002132 5 6374 AC002132 5 6566 AC002132 5 6942 159 AC002132 7 796 AC002132 7 1031 AC002132 7 1068 AC002132 7 1102 2 AC002132 8 307 AC002132 8 628 AC002132 8 666 AC002132 8 806 AC002132 8 891 184 AF008303 1 830 AF008303 1 929 AF008303 1 1081 AF008303 1 1721 6 HSSLIPG 1 41 HSSLIPG 1 63 HSSLIPG 1 151 HSSLIPG 1 616 87 HSSLIPG 2 102 HSSLIPG 2 165 HSSLIPG 2 293 102 HSSLIPG 3 327 HSSLIPG 3 350 24 D67013 1 54 D67013 1 1274 D67013 1 1574 31 D67013 2 186 D67013 2 628 85 D67013 3 97 D67013 3 214 63 D67013 4 254 D67013 4 611 D67013 4 1142 109 D67013 5 66 D67013 5 229 D67013 5 443 D67013 5 525 70 D67013 6 258 D67013 6 364 D67013 6 375 D67013 6 403 D67013 6 407 D67013 6 503 D67013 6 548 13 HUMPREELAS 1 11 HUMPREELAS 1 229 HUMPREELAS 1 473 6 HSRPS7 2 160 118 HSRPS7 3 220 HSRPS7 3 274 HSRPS7 3 489 HSRPS7 3 907 46 HSRPS7 4 25 HSRPS7 4 205 HSRPS7 4 389 HSRPS7 4 399 HSRPS7 4 403 HSRPS7 4 833 HSRPS7 4 845 HSRPS7 4 1154 HSRPS7 4 1481 HSRPS7 4 1657 HSRPS7 4 1682 HSRPS7 4 1809 HSRPS7 4 1813 HSRPS7 4 1882 HSRPS7 4 1969 HSRPS7 4 2070 HSRPS7 4 2153 HSRPS7 4 2174 HSRPS7 4 2299 2 HSRPS7 5 268 HSRPS7 5 310 HSRPS7 5 314 109 HSHFE 1 554 HSHFE 1 663 HSHFE 1 773 HSHFE 1 843 HSHFE 1 1579 HSHFE 1 1818 HSHFE 1 1822 HSHFE 1 2386 HSHFE 1 2485 HSHFE 1 2540 HSHFE 1 2601 HSHFE 1 2697 HSHFE 1 2711 HSHFE 1 2828 HSHFE 1 3257 87 HSHFE 3 88 HSHFE 3 372 HSHFE 3 654 HSHFE 3 784 HSHFE 3 884 162 HSHFE 4 3 HSHFE 4 65 6 HSHFE 5 307 HSHFE 5 450 HSHFE 5 743 HSHFE 5 774 HSHFE 5 866 HSHFE 5 913 6 HUMMGPA 1 231 HUMMGPA 1 976 168 HUMMGPA 2 3 HUMMGPA 2 125 6 HUMLHDC 1 59 HUMLHDC 1 462 HUMLHDC 1 533 HUMLHDC 1 537 HUMLHDC 1 784 HUMLHDC 1 929 HUMLHDC 1 1312 HUMLHDC 1 1474 HUMLHDC 1 1478 HUMLHDC 1 1576 HUMLHDC 1 1976 117 HUMLHDC 2 49 HUMLHDC 2 557 HUMLHDC 2 738 HUMLHDC 2 1021 HUMLHDC 2 1279 HUMLHDC 2 1409 HUMLHDC 2 1447 HUMLHDC 2 2000 HUMLHDC 2 2023 HUMLHDC 2 2478 HUMLHDC 2 2580 HUMLHDC 2 2584 HUMLHDC 2 2982 HUMLHDC 2 3243 HUMLHDC 2 3275 HUMLHDC 2 3313 HUMLHDC 2 3408 HUMLHDC 2 3994 HUMLHDC 2 4395 HUMLHDC 2 4414 169 HUMLHDC 3 205 HUMLHDC 3 485 HUMLHDC 3 493 40 HUMLHDC 4 544 HUMLHDC 4 655 HUMLHDC 4 824 HUMLHDC 4 992 HUMLHDC 4 1189 HUMLHDC 4 1652 HUMLHDC 4 1778 HUMLHDC 4 1955 HUMLHDC 4 1996 64 HUMLHDC 5 81 139 HUMLHDC 6 44 HUMLHDC 6 72 HUMLHDC 6 149 31 HUMLHDC 7 608 HUMLHDC 7 638 HUMLHDC 7 762 HUMLHDC 7 805 57 HUMLHDC 9 1178 HUMLHDC 9 1251 HUMLHDC 9 1563 HUMLHDC 9 1607 HUMLHDC 9 1657 HUMLHDC 9 2176 HUMLHDC 9 2258 HUMLHDC 9 2445 HUMLHDC 9 2980 HUMLHDC 9 3117 HUMLHDC 9 3218 HUMLHDC 9 3603 HUMLHDC 9 3874 124 HUMLHDC 10 100 HUMLHDC 10 113 HUMLHDC 10 303 HUMLHDC 10 318 HUMLHDC 10 566 HUMLHDC 10 738 HUMLHDC 10 821 HUMLHDC 10 896 HUMLHDC 10 947 HUMLHDC 10 1018 HUMLHDC 10 1317 HUMLHDC 10 1469 HUMLHDC 10 2437 HUMLHDC 10 3032 HUMLHDC 10 3367 HUMLHDC 10 3400 HUMLHDC 10 3524 HUMLHDC 10 3826 HUMLHDC 10 3832 HUMLHDC 10 4004 HUMLHDC 10 4484 HUMLHDC 10 4789 160 HSSSPN1AG 1 40 HSSSPN1AG 1 63 175 HSSSPN1AG 3 43 HSSSPN1AG 3 256 HSSSPN1AG 3 470 HSSSPN1AG 3 520 HSSSPN1AG 3 1086 HSSSPN1AG 3 1095 HSSSPN1AG 3 1218 HSSSPN1AG 3 1349 159 HSSSPN1AG 5 26 73 HSHLAA1 3 329 HSHLAA1 3 380 HSHLAA1 3 432 27 HSHLAA1 7 21 HSHLAA1 7 112 90 HSSAA1A 1 798 65 HSSAA1A 2 209 HSSAA1A 2 356 HSSAA1A 2 784 HSSAA1A 2 1331 HSSAA1A 2 1619 HSSAA1A 2 2063 HSSAA1A 2 2157 HSSAA1A 2 2245 HSSAA1A 2 2386 93 HSSAA1A 3 71 HSSAA1A 3 217 HSSAA1A 3 240 2 HSENO2 1 165 HSENO2 1 169 168 HSENO2 3 180 HSENO2 3 222 25 HSENO2 4 257 63 HSENO2 5 81 HSENO2 5 95 HSENO2 5 116 70 HSENO2 6 607 HSENO2 6 639 HSENO2 6 762 HSENO2 6 1200 105 HSENO2 7 92 HSENO2 7 378 HSENO2 7 870 HSENO2 7 1317 117 HSENO2 9 16 HSENO2 9 81 HSENO2 9 133 19 HSATPCP1 1 34 HSATPCP1 1 113 HSATPCP1 1 135 HSATPCP1 1 534 HSATPCP1 1 544 70 HSATPCP1 2 447 HSATPCP1 2 460 HSATPCP1 2 477 HSATPCP1 2 482 HSATPCP1 2 616 13 HSU26425 1 406 HSU26425 1 920 HSU26425 1 929 HSU26425 1 1147 HSU26425 1 1443 HSU26425 1 1672 HSU26425 1 1791 HSU26425 1 2133 HSU26425 1 2138 HSU26425 1 2341 HSU26425 1 2421 HSU26425 1 2450 HSU26425 1 2474 HSU26425 1 2478 349 HSU26425 4 45 85 HSU26425 7 30 HSU26425 8 264 2 HSU26425 9 19 HSU26425 9 33 48 HSU26425 10 496 HSU26425 10 600 HSU26425 10 772 HSU26425 10 777 HSU26425 10 816 HSU26425 10 951 HSU26425 10 1061 HSU26425 10 1197 HSU26425 10 1473 HSU26425 10 1498 HSU26425 10 1552 HSU26425 10 1604 HSU26425 10 1663 HSU26425 10 1677 42 HSU26425 14 115 HSU26425 14 125 HSU26425 14 197 HSU26425 14 253 HSU26425 14 328 HSU26425 14 795 HSU26425 14 835 HSU26425 14 1102 118 HSU26425 15 9 57 HSU26425 19 64 HSU26425 19 178 HSU26425 19 191 HSU26425 19 199 HSU26425 19 373 HSU26425 19 555 HSU26425 19 565 HSU26425 19 573 181 HSU26425 23 22 HSU26425 28 49 2 HSU26425 29 476 HSU26425 29 520 250 HSU26425 30 19 HUMKALLIST 1 90 HUMKALLIST 1 143 HUMKALLIST 1 313 HUMKALLIST 1 867 HUMKALLIST 1 919 HUMKALLIST 1 1021 HUMKALLIST 1 1369 HUMKALLIST 1 1487 27 HUMKALLIST 2 47 HUMKALLIST 2 272 2 HUMKALLIST 3 294 HUMKALLIST 3 352 HUMKALLIST 3 476 HUMKALLIST 3 559 HUMKALLIST 3 627 HUMKALLIST 3 642 106 HSY09781 1 3 HSY09781 1 245 HSY09781 1 665 HSY09781 1 703 HSY09781 1 3159 HSY09781 1 3241 HSY09781 1 3501 HSY09781 1 4002 HSY09781 1 4433 232 HSY09781 2 713 HSY09781 2 774 HSY09781 2 1193 HSY09781 2 1578 HSY09781 2 1908 HSY09781 2 2027 HSY09781 2 2031 HSY09781 2 2049 HSY09781 2 2053 HSY09781 2 2057 HSY09781 2 2061 HSY09781 2 2065 HSY09781 2 2069 HSY09781 2 2683 HSY09781 2 3259 70 HSY09781 3 277 HSY09781 3 300 HSY09781 3 352 HSY09781 3 632 19 HSY09781 5 126 HSY09781 5 197 HSY09781 5 406 HSY09781 5 609 HSY09781 5 654 HSY09781 5 971 HSY09781 5 1321 HSY09781 5 1476 HSY09781 5 3548 HSY09781 5 3767 22 HUMA1GLY2 1 270 HUMA1GLY2 3 58 105 HUMA1GLY2 5 947 148 HSALDOA 2 20 HSALDOA 2 57 HSALDOA 2 235 HSALDOA 2 393 HSALDOA 2 700 HSALDOA 2 882 HSALDOA 2 941 34 HSALDOA 4 163 HSALDOA 4 267 HSALDOA 4 271 202 HSALDOA 5 29 55 HSALDOA 7 16 85 HUMPAP 1 79 HUMPAP 1 84 HUMPAP 1 265 36 HUMPAP 2 25 10 HUMPAP 4 98 HUMPAP 4 174 87 HSPNMTB 1 238 HSPNMTB 1 305 HSPNMTB 1 342 HSPNMTB 1 680 HSPNMTB 1 887 48 HSPNMTB 2 13 2 HSU05259 1 31 HSU05259 1 168 HSU05259 1 394 HSU05259 1 1268 HSU05259 1 1308 HSU05259 1 1390 114 HSU05259 2 88 HSU05259 2 173 60 HSU05259 3 341 HSU05259 3 626 127 AF017257 1 121 AF017257 1 190 AF017257 1 261 AF017257 1 726 AF017257 1 772 AF017257 1 856 AF017257 1 1565 AF017257 1 1587 AF017257 1 1707 AF017257 1 2231 AF017257 1 2369 AF017257 1 2460 AF017257 1 2837 94 AF017257 2 78 AF017257 2 167 AF017257 2 575 AF017257 2 714 AF017257 2 792 81 AF017257 3 29 168 AF017257 4 71 AF017257 4 142 AF017257 4 189 AF017257 4 512 AF017257 4 674 AF017257 4 737 AF017257 4 901 AF017257 4 1401 AF017257 4 1458 9 AF017257 5 122 AF017257 5 151 AF017257 5 403 AF017257 5 457 AF017257 5 1273 12 AF017257 6 347 AF017257 6 755 AF017257 6 830 192 AF017257 7 436 AF017257 7 487 AF017257 7 783 156 AF017257 8 118 AF017257 8 454 AF017257 8 650 121 HSIL1AG 1 432 HSIL1AG 1 740 HSIL1AG 1 862 2 HSIL1AG 2 140 HSIL1AG 2 258 HSIL1AG 2 303 HSIL1AG 2 360 HSIL1AG 2 415 HSIL1AG 2 723 10 HSIL1AG 3 120 HSIL1AG 3 520 HSIL1AG 3 991 HSIL1AG 3 1016 HSIL1AG 3 1253 HSIL1AG 3 1789 93 HSIL1AG 4 950 HSIL1AG 4 1028 HSIL1AG 4 1170 HSIL1AG 4 1232 HSIL1AG 4 1247 186 HSIL1AG 5 84 HSIL1AG 5 569 HSIL1AG 5 573 HSIL1AG 5 585 HSIL1AG 5 1495 HSIL1AG 5 1838 HSIL1AG 5 1852 HSIL1AG 5 1934 52 HUMPP14B 1 183 4 HUMPP14B 2 67 HUMPP14B 2 239 17 HUMPP14B 3 224 HUMPP14B 3 258 HUMPP14B 3 319 HUMPP14B 3 327 HUMPP14B 3 335 HUMPP14B 3 339 HUMPP14B 3 343 HUMPP14B 3 347 HUMPP14B 3 351 HUMPP14B 3 378 HUMPP14B 3 382 HUMPP14B 3 390 HUMPP14B 3 394 HUMPP14B 3 398 HUMPP14B 3 406 HUMPP14B 3 414 HUMPP14B 3 418 HUMPP14B 3 430 HUMPP14B 3 438 HUMPP14B 3 446 HUMPP14B 3 454 HUMPP14B 3 462 HUMPP14B 3 470 HUMPP14B 3 478 HUMPP14B 3 486 HUMPP14B 3 494 HUMPP14B 3 502 HUMPP14B 3 506 HUMPP14B 3 510 HUMPP14B 3 514 HUMPP14B 3 534 HUMPP14B 3 538 HUMPP14B 3 550 HUMPP14B 3 558 HUMPP14B 3 574 HUMPP14B 3 578 HUMPP14B 3 598 HUMPP14B 3 610 HUMPP14B 3 614 HUMPP14B 3 622 HUMPP14B 3 626 HUMPP14B 3 630 HUMPP14B 3 634 HUMPP14B 3 638 HUMPP14B 3 646 HUMPP14B 3 654 HUMPP14B 3 662 HUMPP14B 3 670 HUMPP14B 3 1081 45 HUMPP14B 4 26 HUMPP14B 4 30 HUMPP14B 4 696 HUMPP14B 4 727 18 HUMPP14B 5 90 HUMPP14B 5 154 57 HSTUBAG 1 300 HSTUBAG 1 365 HSTUBAG 1 1375 109 HSTUBAG 2 22 HSTUBAG 2 49 HSTUBAG 3 22 25 HSTUBAG 2 3 97 HUMLYTOXBB 1 215 HUMLYTOXBB 1 272 160 HSMOGG 1 658 HSMOGG 1 1202 HSMOGG 1 1599 HSMOGG 1 1679 HSMOGG 1 1683 114 HSMOGG 2 220 HSMOGG 2 623 HSMOGG 2 639 HSMOGG 2 950 HSMOGG 2 1142 HSMOGG 2 1252 HSMOGG 2 1277 HSMOGG 2 1376 HSMOGG 2 1431 HSMOGG 2 1584 HSMOGG 2 2300 HSMOGG 2 2755 HSMOGG 2 2961 HSMOGG 2 4116 HSMOGG 2 4146 HSMOGG 2 4815 HSMOGG 2 5098 HSMOGG 2 5704 HSMOGG 2 6209 HSMOGG 2 6465 6 HSMOGG 3 13 HSMOGG 3 81 39 HSMOGG 4 131 HSMOGG 4 158 165 HSMOGG 5 290 HSMOGG 5 334 HSMOGG 5 674 HSMOGG 5 1231 HSMOGG 5 1601 HSMOGG 5 1763 HSMOGG 5 1795 HSMOGG 5 2296 18 HSARYLA 4 90 HSARYLA 4 236 86 HSARYLA 6 57 HSARYLA 6 195 229 HUMPCI 1 156 HUMPCI 1 640 HUMPCI 1 1034 HUMPCI 1 1251 HUMPCI 1 1395 HUMPCI 1 1570 84 HUMPCI 2 376 29 HSCST3G 1 581 HSCST3G 1 591 HSCST3G 1 905 HSCST3G 1 1013 HSCST3G 1 1735 HSCST3G 1 1826 HSCST3G 1 1830 HSCST3G 1 2094 HSCST3G 1 2114 HSCST3G 1 2139 175 HSCST3G 2 45 HSCST3G 2 88 HSCST3G 2 150 HSCST3G 2 170 HSCST3G 2 184 HSCST3G 2 188 HSCST3G 2 233 HSCST3G 2 239 HSCST3G 2 243 HSCST3G 2 253 HSCST3G 2 368 HSCST3G 2 428 HSCST3G 2 434 HSCST3G 2 456 HSCST3G 2 1118 70 HUMGSTM4A 2 132 HUMGSTM4A 2 395 135 HUMGSTM4A 3 212 49 HUMGSTM4A 4 73 HUMGSTM4A 5 347 HUMGSTM4A 5 699 HUMGSTM4A 5 797 97 HUMGSTM4A 7 236 HUMGSTM4A 7 585 HUMGSTM4A 7 847 HUMGSTM4A 7 961 HUMGSTM4A 7 1102 HUMGSTM4A 7 1296 HUMGSTM4A 7 1334 HUMGSTM4A 7 1449 HUMGSTM4A 7 1527 163 HUMIL4A 2 1183 HUMIL4A 2 1342 HUMIL4A 2 1370 HUMIL4A 2 1390 HUMIL4A 2 1418 HUMIL4A 2 1607 HUMIL4A 2 1627 HUMIL4A 2 1741 HUMIL4A 2 1753 HUMIL4A 2 2250 HUMIL4A 2 2410 HUMIL4A 2 2838 HUMIL4A 2 3203 HUMIL4A 2 3370 HUMIL4A 2 3467 HUMIL4A 2 4007 HUMIL4A 2 5075 58 HUMIL4A 3 429 HUMIL4A 3 510 HUMIL4A 3 629 HUMIL4A 3 642 HUMIL4A 3 662 HUMIL4A 3 911 HUMIL4A 3 977 HUMIL4A 3 1037 HUMIL4A 3 1131 HUMIL4A 3 1136 HUMIL4A 3 1204 HUMIL4A 3 1312 HUMIL4A 3 1403 HUMIL4A 3 1457 HUMIL4A 3 1462 HUMIL4A 3 1508 HUMIL4A 3 1519 HUMIL4A 3 2365 HUMIL4A 3 2396 HUMIL4A 3 2497 76 HUMTHY1A 1 93 HUMTHY1A 1 164 HUMTHY1A 1 420 96 HUMTHY1A 2 25 15 HUMRIGBCHA 1 549 HUMRIGBCHA 1 699 HUMRIGBCHA 1 735 2 HUMRIGBCHA 3 124 HUMRIGBCHA 3 187 HUMRIGBCHA 3 452 HUMRIGBCHA 3 466 HUMRIGBCHA 3 744 HUMRIGBCHA 3 856 HUMRIGBCHA 3 993 HUMRIGBCHA 3 1140 HUMRIGBCHA 3 1385 HUMRIGBCHA 3 1736 HUMRIGBCHA 3 1921 HUMRIGBCHA 3 1963 HUMRIGBCHA 3 2056 HUMRIGBCHA 3 2191 HUMRIGBCHA 3 2204 16 HUMRIGBCHA 5 46 HUMRIGBCHA 5 50 HUMRIGBCHA 5 124 HUMRIGBCHA 5 363 49 HUMRIGBCHA 6 242 HUMRIGBCHA 6 296 HUMRIGBCHA 6 813 HUMRIGBCHA 6 976 HUMRIGBCHA 6 1409 HUMRIGBCHA 6 1451 19 HSMICAGEN 1 61 HSMICAGEN 1 1728 HSMICAGEN 1 1813 HSMICAGEN 1 2096 HSMICAGEN 1 3118 HSMICAGEN 1 3279 HSMICAGEN 1 3767 HSMICAGEN 1 4273 HSMICAGEN 1 4308 HSMICAGEN 1 4747 HSMICAGEN 1 4860 HSMICAGEN 1 4940 HSMICAGEN 1 5072 HSMICAGEN 1 5410 HSMICAGEN 1 5621 HSMICAGEN 1 5633 288 HSMICAGEN 2 105 HSMICAGEN 2 118 HSMICAGEN 2 140 HSMICAGEN 2 229 24 HSMICAGEN 3 241 HSMICAGEN 3 470 129 HSMICAGEN 5 28 HSMICAGEN 5 222 HSMICAGEN 5 311 HSMICAGEN 5 316 HSMICAGEN 5 965 HSMICAGEN 5 1112 HSMICAGEN 5 1199 HSMICAGEN 5 1264 HSMICAGEN 5 1355 HSMICAGEN 5 1966 HSMICAGEN 5 1985 HSMICAGEN 5 2153 HSMICAGEN 5 2161 51 HSU04636 1 116 HSU04636 1 305 HSU04636 1 430 144 HSU04636 3 226 HSU04636 3 361 57 HSU04636 5 285 HSU04636 5 356 7 HSU04636 7 90 HSU04636 7 128 48 HSU04636 8 359 HSU04636 8 363 133 AF037372 1 95 AF037372 1 601 52 AF037372 3 56 AF037372 3 197 129 HSASML 1 195 HSASML 1 329 64 HSASML 2 39 HSASML 2 948 98 HSASML 4 33 2 D83195 2 28 23 D83195 3 91 D83195 3 169 D83195 3 225 D83195 3 281 11 D83195 4 189 174 D83195 7 50 28 AB002059 1 45 AB002059 1 363 AB002059 1 383 AB002059 1 475 2 AB002059 2 277 AB002059 2 1065 55 AB002059 3 86 AB002059 3 357 AB002059 3 518 AB002059 3 1486 AB002059 3 1613 AB002059 3 2483 AB002059 3 2656 AB002059 3 2660 AB002059 3 2765 AB002059 3 2807 AB002059 3 2839 AB002059 3 2853 AB002059 3 2861 AB002059 3 2903 AB002059 3 2930 AB002059 3 2935 AB002059 3 3001 AB002059 3 3321 AB002059 3 3434 AB002059 3 3919 AB002059 3 4029 AB002059 3 4069 AB002059 3 4178 AB002059 3 4215 AB002059 3 4488 AB002059 3 4503 AB002059 3 4588 232 AB002059 8 105 AB002059 8 572 AB002059 8 1049 AB002059 8 1091 AB002059 8 1184 AB002059 8 1500 AB002059 8 1542 AB002059 8 1889 2 AB002059 9 9 85 AB002059 10 34 AB002059 10 53 37 HUMCAPG 1 283 HUMCAPG 1 519 6 HUMCAPG 2 113 2 HUMCAPG 3 59 HUMCAPG 4 208 181 HSU16720 1 165 HSU16720 1 223 HSU16720 1 325 HSU16720 1 581 46 HSU16720 2 185 40 HSU16720 3 230 HSU16720 3 825 274 HSU16720 4 239 HSU16720 4 490 HSU16720 4 502 HSU16720 4 661 HSU16720 4 801 HSU16720 4 909 187 HSCLN3 1 120 HSCLN3 2 489 HSCLN3 2 514 HSCLN3 2 518 HSCLN3 2 530 HSCLN3 2 974 HSCLN3 2 1155 HSCLN3 2 1249 HSCLN3 2 1673 HSCLN3 2 2005 2 HSCLN3 3 3 HSCLN3 3 28 HSCLN3 3 64 HSCLN3 3 509 49 HSCLN3 4 166 52 HSCLN3 5 5 8 HSCLN3 6 218 HSCLN3 6 766 111 HSCLN3 8 123 HSCLN3 8 189 HSCLN3 8 438 HSCLN3 8 440 HSCLN3 8 555 HSCLN3 8 595 HSCLN3 8 1172 HSCLN3 8 1246 HSCLN3 8 1459 HSCLN3 8 1548 HSCLN3 8 1656 2 HSCLN3 9 24 HSCLN3 9 93 HSCLN3 9 613 HSCLN3 9 831 HSCLN3 9 975 HSCLN3 9 1110 HSCLN3 9 1214 69 HSCLN3 10 17 HSCLN3 11 3 16 HSCLN3 13 200 HSCLN3 13 330 HSCLN3 13 724 HSCLN3 13 768 HSCLN3 13 889 HSCLN3 13 1061 HSCLN3 13 1171 HSCLN3 13 1198 HSCLN3 13 1340 HSCLN3 13 1460 HSCLN3 13 1474 HSCLN3 13 1907 HSCLN3 13 2111 HSCLN3 13 2165 HSCLN3 13 2469 HSCLN3 13 2745 HSCLN3 13 2787 HSCLN3 13 2813 HSCLN3 13 2876 HSCLN3 13 2989 HSCLN3 13 3036 HSCLN3 13 3083 HSCLN3 13 3613 HSCLN3 13 3882 HSCLN3 13 4024 HSCLN3 13 4066 229 HSU66711 1 301 156 HSCDIR2 2 366 21 HSCDIR2 3 148 42 HUMEPOHYDD 1 43 HUMEPOHYDD 1 340 HUMEPOHYDD 1 458 HUMEPOHYDD 1 620 HUMEPOHYDD 1 632 HUMEPOHYDD 1 765 HUMEPOHYDD 1 880 HUMEPOHYDD 1 885 HUMEPOHYDD 1 942 HUMEPOHYDD 1 1407 HUMEPOHYDD 1 2303 HUMEPOHYDD 1 2560 325 HUMEPOHYDD 2 31 HUMEPOHYDD 2 62 HUMEPOHYDD 2 110 HUMEPOHYDD 2 348 HUMEPOHYDD 2 435 HUMEPOHYDD 2 631 HUMEPOHYDD 2 1345 HUMEPOHYDD 2 1610 HUMEPOHYDD 2 1622 HUMEPOHYDD 2 1695 HUMEPOHYDD 2 1778 HUMEPOHYDD 2 1924 HUMEPOHYDD 2 2585 HUMEPOHYDD 2 3075 HUMEPOHYDD 2 3135 HUMEPOHYDD 2 3408 HUMEPOHYDD 2 3712 HUMEPOHYDD 2 3871 HUMEPOHYDD 2 4122 HUMEPOHYDD 2 4227 HUMEPOHYDD 2 4231 HUMEPOHYDD 2 4406 HUMEPOHYDD 2 4544 HUMEPOHYDD 2 4719 HUMEPOHYDD 2 5107 HUMEPOHYDD 2 5118 HUMEPOHYDD 2 5227 HUMEPOHYDD 2 5471 HUMEPOHYDD 2 5723 HUMEPOHYDD 2 5798 HUMEPOHYDD 2 5909 HUMEPOHYDD 2 6530 117 HUMEPOHYDD 3 84 24 HUMEPOHYDD 4 4 HUMEPOHYDD 4 19 HUMEPOHYDD 4 238 2 HUMEPOHYDD 5 299 HUMEPOHYDD 5 304 HUMEPOHYDD 5 462 HUMEPOHYDD 5 713 HUMEPOHYDD 5 735 HUMEPOHYDD 5 1013 HUMEPOHYDD 5 1034 HUMEPOHYDD 5 1478 HUMEPOHYDD 5 1520 HUMEPOHYDD 5 1797 HUMEPOHYDD 5 1950 HUMEPOHYDD 5 2168 156 HUMEPOHYDD 6 168 HUMEPOHYDD 6 366 HUMEPOHYDD 6 493 HUMEPOHYDD 6 1113 HUMEPOHYDD 6 1340 HUMEPOHYDD 6 1478 HUMEPOHYDD 6 1515 HUMEPOHYDD 6 1652 HUMEPOHYDD 6 1678 HUMEPOHYDD 6 1749 HUMEPOHYDD 6 1774 HUMEPOHYDD 6 1789 2 HUMEPOHYDD 7 152 HUMEPOHYDD 7 184 HUMEPOHYDD 7 293 2 HSRPS3AGE 1 244 2 HSRPS3AGE 3 296 HSRPS3AGE 3 445 HSRPS3AGE 3 849 HSRPS3AGE 3 1083 HSRPS3AGE 3 1426 HSRPS3AGE 3 1518 HSRPS3AGE 3 1532 HSRPS3AGE 3 1540 19 HSRPS3AGE 4 81 HSRPS3AGE 4 87 HSRPS3AGE 4 411 HSRPS3AGE 4 907 HSRPS3AGE 4 941 HSRPS3AGE 4 989 2 HSRPS3AGE 5 3 6 HUMBETGLOA 2 291 HUMBETGLOA 2 480 HUMBETGLOA 2 704 19 HSEOTAX 1 27 HSEOTAX 1 32 HSEOTAX 1 55 HSEOTAX 1 418 HSEOTAX 1 929 30 HSEOTAX 2 3 HSEOTAX 2 136 2 HSRPS8 2 156 76 HSRPS8 3 133 HSRPS8 3 265 HSRPS8 3 397 HSRPS8 3 575 HSRPS8 3 674 6 HSRPS8 5 22 HSRPS8 5 298 HSRPS8 5 313 42 HUMHIS102 1 154 HUMHIS102 1 747 91 HUMHIS102 3 350 HUMHIS102 3 644 HUMHIS102 3 748 139 HSU91522 1 241 10 HSU91522 2 216 HSU91522 2 264 HSU91522 2 329 HSU91522 2 333 HSU91522 2 524 HSU91522 2 682 HSU91522 2 769 2 HSE48ATGN 1 702 78 HSE48ATGN 2 80 HSE48ATGN 2 93 6 HUMPHOSA 1 78 HUMPHOSA 1 191 2 HUMPHOSA 2 68 HUMPHOSA 2 401 27 HUMPHOSA 3 60 63 HUMPHOSA 7 253 HUMPHOSA 7 290 60 HUMCFVII 1 356 HUMCFVII 1 366 HUMCFVII 1 537 HUMCFVII 1 542 HUMCFVII 1 552 HUMCFVII 1 617 HUMCFVII 1 631 HUMCFVIT 1 732 HUMCFVII 1 766 HUMCFVII 1 890 153 HUMCFVII 2 992 HUMCFVII 2 1077 HUMCFVII 2 1244 1080 HUMCFVII 3 159 HUMCFVII 3 371 HUMCFVII 3 1481 HUMCFVII 3 1854 HUMCFVII 3 1891 274 HUMCFVII 5 97 HUMCFVII 5 146 HUMCFVII 5 841 156 HUMCFVII 6 132 HUMCFVII 6 675 HUMCFVII 6 699 30 HUMCFVII 7 90 HUMCFVII 7 276 HUMCFVII 7 344 HUMCFVII 7 562 199 HUMCFVII 8 36 HUMCFVII 8 73 HUMCFVII 8 110 HUMCFVII 8 147 HUMCFVII 8 184 HUMCFVII 8 484 HUMCFVII 8 765 366 HSU19765 2 46 69 HSU19765 3 133 HSU19765 3 237 HSU19765 3 341 HSU19765 3 438 2 HUMMHDC3B 1 170 HUMMHDC3B 1 273 HUMMHDC3B 1 780 HUMMHDC3B 1 840 HUMMHDC3B 1 900 HUMMHDC3B 1 930 HUMMHDC3B 1 954 HUMMHDC3B 1 1406 162 HUMMHDC3B 2 155 HUMMHDC3B 2 581 HUMMHDC3B 2 629 HUMMHDC3B 2 719 HUMMHDC3B 2 1038 HUMMHDC3B 2 1185 HUMMHDC3B 2 1686 HUMMHDC3B 2 2291 HUMMHDC3B 2 2480 HUMMHDC3B 2 2703 87 HUMMHDC3B 3 261 90 HUMMHDC3B 4 427 HUMMHDC3B 4 505 HUMMHDC3B 4 989 72 HSHLADMBG 1 49 HSHLADMBG 1 148 HSHLADMBG 1 292 HSHLADMBG 1 377 HSHLADMBG 1 547 HSHLADMBG 1 931 120 HSHLADMBG 2 165 HSHLADMBG 2 174 HSHLADMBG 2 203 HSHLADMBG 2 508 HSHLADMBG 2 746 HSHLADMBG 2 781 HSHLADMBG 2 1121 93 HSHLADMBG 3 174 HSHLADMBG 3 186 HSHLADMBG 3 313 HSHLADMBG 3 348 HSHLADMBG 3 1106 HSHLADMBG 3 1144 HSHLADMBG 3 1225 HSHLADMBG 3 1444 HSHLADMBG 3 1474 HSHLADMBG 3 1497 27 HSHLADMBG 5 59 HSHLADMBG 5 97 HSHLADMBG 5 217 54 HUMHPARS1 1 253 HUMHPARS1 1 582 HUMHPARS1 1 608 HUMHPARS1 1 914 HUMHPARS1 1 958 HUMHPARS1 1 1301 HUMHPARS1 1 1315 HUMHPARS1 1 1402 HUMHPARS1 1 1428 83 HUMHPARS1 3 75 HUMHPARS1 3 237 HUMHPARS1 3 316 60 HUMHPARS1 4 159 9 HUMHPARS1 5 75 HUMHPARS1 5 237 HUMHPARS1 5 316 60 HUMHPARS1 6 152 HUMHPARS1 6 795 9 HSIFNAR 1 38 HSIFNAR 1 359 HSIFNAR 1 525 HSIFNAR 1 573 HSIFNAR 1 709 HSIFNAR 1 766 HSIFNAR 1 1334 HSIFNAR 1 1781 HSIFNAR 1 1865 HSIFNAR 1 1976 HSIFNAR 1 2147 HSIFNAR 1 2325 HSIFNAR 1 2748 HSIFNAR 1 2772 HSIFNAR 1 3272 HSIFNAR 1 3352 HSIFNAR 1 3650 HSIFNAR 1 3781 HSIFNAR 1 4555 HSIFNAR 1 4817 HSIFNAR 1 4881 HSIFNAR 1 5012 HSIFNAR 1 6867 HSIFNAR 1 7145 HSIFNAR 1 7281 HSIFNAR 1 7351 HSIFNAR 1 7738 HSIFNAR 1 7763 HSIFNAR 1 8388 HSIFNAR 1 8421 HSIFNAR 1 8936 HSIFNAR 1 9030 HSIFNAR 1 9197 HSIFNAR 1 9439 HSIFNAR 1 9592 HSIFNAR 1 9846 HSIFNAR 1 9969 HSIFNAR 1 10195 HSIFNAR 1 10296 276 HSIFNAR 2 3 HSIFNAR 2 329 HSIFNAR 2 338 HSIFNAR 2 397 HSIFNAR 2 2502 HSIFNAR 2 2558 HSIFNAR 2 2680 HSIFNAR 2 2724 HSIFNAR 2 2846 HSIFNAR 2 3110 HSIFNAR 2 3467 HSIFNAR 2 3732 HSIFNAR 2 3833 HSIFNAR 2 4061 HSIFNAR 2 4138 HSIFNAR 2 4156 HSIFNAR 2 4736 HSIFNAR 2 4758 32 HSIFNAR 3 603 HSIFNAR 3 736 HSIFNAR 3 997 HSIFNAR 3 1449 81 HSIFNAR 4 31 25 HSIFNAR 5 91 HSIFNAR 5 247 HSIFNAR 5 556 HSIFNAR 5 593 HSIFNAR 5 645 HSIFNAR 5 903 HSIFNAR 5 1352 HSIFNAR 5 1394 21 HSIFNAR 6 106 HSIFNAR 6 128 HSIFNAR 6 997 HSIFNAR 6 1050 HSIFNAR 6 1167 HSIFNAR 6 1205 HSIFNAR 6 1405 HSIFNAR 6 1453 HSIFNAR 6 1511 HSIFNAR 6 1586 HSIFNAR 6 1868 HSIFNAR 6 1910 HSIFNAR 6 2003 HSIFNAR 6 2236 HSIFNAR 6 2633 HSIFNAR 6 2650 HSIFNAR 6 3208 HSIFNAR 6 3212 HSIFNAR 6 3226 HSIFNAR 6 3609 2 HSIFNAR 8 53 HSIFNAR 8 392 HSIFNAR 8 462 HSIFNAR 8 970 HSIFNAR 8 1135 HSIFNAR 8 1577 HSIFNAR 8 1647 HSIFNAR 8 1686 HSIFNAR 8 1921 HSIFNAR 8 2429 HSIFNAR 8 2565 HSIFNAR 8 2637 HSIFNAR 8 2827 HSIFNAR 8 2957 HSIFNAR 8 3174 28 HSIFNAR 9 49 HSIFNAR 9 338 HSIFNAR 9 552 33 HSIFNAR 10 330 HSIFNAR 10 344 HSIFNAR 10 563 HSIFNAR 10 581 HSIFNAR 10 648 HSIFNAR 10 659 HSIFNAR 10 897 HSIFNAR 10 934 HSIFNAR 10 1394 HSIFNAR 10 1443 34 HUMPDHAL 1 184 HUMPDHAL 1 269 HUMPDHAL 1 692 HUMPDHAL 1 782 HUMPDHAL 1 848 HUMPDHAL 1 1144 HUMPDHAL 1 1152 HUMPDHAL 1 1250 HUMPDHAL 1 1265 HUMPDHAL 1 1591 HUMPDHAL 1 1725 HUMPDHAL 1 1740 HUMPDHAL 1 2525 HUMPDHAL 1 2762 HUMPDHAL 1 2766 HUMPDHAL 1 2935 HUMPDHAL 1 3074 HUMPDHAL 1 3754 HUMPDHAL 1 3868 HUMPDHAL 1 3963 HUMPDHAL 1 3968 HUMPDHAL 1 4019 HUMPDHAL 1 4626 HUMPDHAL 1 4640 193 HUMPDHAL 2 158 46 HUMPDHAL 3 6 HUMPDHAL 3 10 HUMPDHAL 3 108 HUMPDHAL 3 162 97 HUMPDHAL 4 192 HUMPDHAL 4 209 HUMPDHAL 4 282 HUMPDHAL 4 316 HUMPDHAL 4 482 HUMPDHAL 4 617 HUMPDHAL 4 1055 HUMPDHAL 4 1445 HUMPDHAL 4 1535 30 HUMPDHAL 5 327 HUMPDHAL 5 352 HUMPDHAL 5 519 HUMPDHAL 5 543 HUMPDHAL 5 561 HUMPDHAL 5 825 HUMPDHAL 5 1089 HUMPDHAL 5 1160 31 HUMPDHAL 6 95 79 HUMPDHAL 7 48 124 HUMPDHAL 8 102 HUMPDHAL 8 268 HUMPDHAL 8 384 HUMPDHAL 8 487 HUMPDHAL 8 627 HUMPDHAL 8 645 HUMPDHAL 8 702 HUMPDHAL 8 1265 HUMPDHAL 8 1446 10 HUMPDHAL 9 405 HUMPDHAL 9 927 41 HUMPPPA 1 181 HUMPPPA 1 197 104 HUMPDHBET 2 410 HUMPDHBET 2 1192 HUMPDHBET 2 1228 HUMPDHBET 2 1569 259 HUMPDHBET 3 34 HUMPDHBET 5 384 HUMPDHBET 5 388 19 HUMPDHBET 6 189 HUMPDHBET 6 379 36 HUMPDHBET 7 160 HUMPDHBET 7 164 33 HUMPDHBET 8 77 HUMPDHBET 8 178 HUMPDHBET 8 621 HUMPDHBET 8 739 73 HUMPDHBET 9 120 123 HSU52427 2 245 2 HSU52427 3 206 HSU52427 3 683 HSU52427 3 716 HSU52427 3 952 HSU52427 3 1164 HSU52427 3 1204 HSU52427 3 1306 HSU52427 3 1438 HSU52427 3 1446 HSU52427 3 1674 31 HSU52427 5 182 HSU52427 5 193 196 HSU52427 6 339 HSU52427 6 464 163 AF006501 1 289 AF006501 1 356 AF006501 1 372 AF006501 1 408 AF006501 1 818 AF006501 1 855 AF006501 1 927 AF006501 1 994 AF006501 1 1085 AF006501 1 1104 AF006501 1 1125 AF006501 1 2157 AF006501 1 2191 AF006501 1 2383 AF006501 1 2939 2 AF006501 2 58 AF006501 2 299 AF006501 2 343 AF006501 2 496 AF006501 2 537 AF006501 2 569 AF006501 2 594 AF006501 2 642 AF006501 2 1610 AF006501 2 1804 AF006501 2 1846 AF006501 2 2007 AF006501 2 2011 AF006501 2 2121 AF006501 2 2261 AF006501 2 2315 61 AF006501 3 294 AF006501 3 426 AF006501 3 452 AF006501 3 600 AF006501 3 1200 AF006501 3 1725 AF006501 3 1812 AF006501 3 1886 AF006501 3 1898 AF006501 3 2301 AF006501 3 2414 AF006501 3 2536 AF006501 3 3620 AF006501 3 3759 AF006501 3 3949 AF006501 3 4097 AF006501 3 4403 AF006501 3 4421 AF006501 3 4680 AF006501 3 4781 AF006501 3 4828 AF006501 3 4971 AF006501 3 5342 AF006501 3 5551 AF006501 3 5776 AF006501 3 5858 AF006501 3 6031 AF006501 3 6097 AF006501 3 6546 AF006501 3 6923 AF006501 3 6949 AF006501 3 7540 2 HSMTS1G 1 18 HSMTS1G 1 199 HSMTS1G 1 247 HSMTS1G 1 263 HSMTS1G 1 511 10 HSU43572 1 606 HSU43572 1 663 425 HSU43572 2 52 199 HSU43572 4 152 HSU43572 4 307 HSU43572 4 992 HSU43572 4 1723 2 HSU43572 5 61 HSU43572 5 179 HSU43572 5 412 HSU43572 5 1058 HSU43572 5 1134 HSU43572 5 1226 HSU43572 5 1387 HSU43572 5 1564 HSU43572 5 1616 105 HUMGALT54X 1 235 HUMGALT54X 1 239 57 HSU20325 1 247 HSU20325 1 413 352 HSU20325 2 4 HSU20325 2 98 HSU20325 2 142 HSU20325 2 183 HSU20325 2 334 88 HUMGRP78 2 34 HUMGRP78 2 110 181 HUMGRP78 6 189 27 HUMGRP78 7 123 HUMGRP78 7 388 HUMGRP78 7 955 21 HS370M22 1 3 HS370M22 1 209 HS370M22 1 288 HS370M22 1 300 HS370M22 1 368 HS370M22 1 915 HS370M22 1 944 HS370M22 1 1225 HS370M22 1 2029 HS370M22 1 2182 HS370M22 1 2554 HS370M22 1 3399 HS370M22 1 3558 HS370M22 1 3616 HS370M22 1 3649 HS370M22 1 4806 HS370M22 1 4826 HS370M22 1 5077 HS370M22 1 5168 HS370M22 1 5718 HS370M22 1 6567 HS370M22 1 7562 HS370M22 1 7610 HS370M22 1 7946 HS370M22 1 8453 HS370M22 1 8483 79 HS370M22 2 302 HS370M22 2 700 HS370M22 2 793 HS370M22 2 835 HS370M22 2 1268 HS370M22 2 1383 HS370M22 2 1740 HS370M22 2 2532 HS370M22 2 2553 HS370M22 2 2714 HS370M22 2 2884 HS370M22 2 3032 HS370M22 2 3320 HS370M22 2 3615 HS370M22 2 3838 HS370M22 2 3941 2 HS370M22 3 198 HS370M22 3 249 HS370M22 3 328 HS370M22 3 670 HS370M22 3 731 HS370M22 3 744 HS370M22 3 1403 HS370M22 3 1727 HS370M22 3 2394 HS370M22 3 2825 HS370M22 3 3386 HS370M22 3 3611 HS370M22 3 3627 HS370M22 3 3868 HS370M22 3 3963 HS370M22 3 4114 HS370M22 3 4882 HS370M22 3 4987 HS370M22 3 5064 HS370M22 3 5543 HS370M22 3 5597 HS370M22 3 5692 HS370M22 3 5746 5 HS370M22 4 132 HS370M22 4 814 HS370M22 4 954 HS370M22 4 2113 HS370M22 4 3009 HS370M22 4 3013 HS370M22 4 3083 HS370M22 4 3136 HS370M22 4 3426 HS370M22 4 3527 HS370M22 4 3541 HS370M22 4 3804 HS370M22 4 4091 HS370M22 4 4415 HS370M22 4 4453 130 S63697 1 11 S63697 1 154 S63697 1 223 34 S63697 2 64 6 HUMMCHEMP 1 115 HUMMCHEMP 1 137 HUMMCHEMP 1 309 HUMMCHEMP 1 313 HUMMCHEMP 1 390 HUMMCHEMP 1 402 24 HSU12421 1 3 HSU12421 1 271 HSU12421 1 903 HSU12421 1 1088 HSU12421 1 1394 HSU12421 1 1570 2 HSU12421 2 77 HSU12421 2 174 HSU12421 2 210 HSU12421 2 353 HSU12421 2 395 HSU12421 2 543 HSU12421 2 857 HSU12421 2 1135 HSU12421 2 1161 HSU12421 2 1268 HSU12421 2 1470 HSU12421 2 1492 70 HUMIL1B 1 124 HUMIL1B 1 332 HUMIL1B 1 435 29 HUMIL1B 2 760 HUMIL1B 2 1251 HUMIL1B 2 1354 16 HUMIL1B 3 256 6 HUMIL1B 4 434 81 HUMIL1B 5 3 HUMIL1B 5 129 HUMIL1B 5 440 127 HUMV2R 1 95 HUMV2R 1 213 HUMV2R 1 269 69 HUMHMG2A 1 35 HUMHMG2A 1 240 70 HUMHMG2A 3 44 HUMHMG2A 3 146 19 HUMSPBAA 1 239 HUMSPBAA 1 261 48 HUMSPBAA 3 271 67 HUMSPBAA 5 100 103 HUMSPBAA 6 179 HUMSPBAA 6 553 HUMSPBAA 6 574 HUMSPBAA 6 669 HUMSPBAA 6 845 HUMSPBAA 6 896 HUMSPBAA 6 957 HUMSPBAA 6 1151 HUMSPBAA 6 1165 HUMSPBAA 6 1213 HUMSPBAA 6 1251 115 HUMSPBAA 8 150 HUMSPBAA 8 379 55 HUMSPBAA 9 288 HUMSPBAA 9 409 160 HUMCEL 1 207 HUMCEL 1 295 HUMCEL 1 313 HUMCEL 1 393 HUMCEL 1 468 HUMCEL 1 593 HUMCEL 1 630 HUMCEL 1 1572 HUMCEL 1 1715 HUMCEL 1 1719 HUMCEL 1 1870 145 HUMCEL 2 40 HUMCEL 4 20 HUMCEL 4 233 HUMCEL 4 373 HUMCEL 4 391 HUMCEL 4 544 HUMCEL 4 943 18 HUMCEL 7 36 HUMCEL 7 267 6 HUMCEL 8 134 2 HUMCEL 9 86 HUMCEL 9 481 HUMCEL 9 499 HUMCEL 9 723 HUMCEL 9 967 HUMCEL 9 990 HUMCEL 9 1088 2 HUMCEL 10 6 HUMCEL 10 131 2 HSCEATG 1 539 HSCEATG 1 544 HSCEATG 1 587 HSCEATG 1 656 81 HSQC8B6 1 1346 HSQC8B6 1 1887 HSQC8B6 1 1904 HSQC8B6 1 2110 HSQC8B6 1 2513 HSQC8B6 1 2604 HSQC8B6 1 3017 HSQC8B6 1 3308 HSQC8B6 1 3450 HSQC8B6 1 3602 HSQC8B6 1 3969 HSQC8B6 1 4462 HSQC8B6 1 4593 HSQC8B6 1 4917 HSQC8B6 1 4997 HSQC8B6 1 5795 HSQC8B6 1 5804 HSQC8B6 1 5831 HSQC8B6 1 5935 HSQC8B6 1 5942 HSQC8B6 1 5983 HSQC8B6 1 6184 138 HSQC8B6 2 471 HSQC8B6 2 677 HSQC8B6 2 923 HSQC8B6 2 1093 HSQC8B6 2 1354 HSQC8B6 2 1584 HSQC8B6 2 1834 96 HSQC8B6 3 585 HSQC8B6 3 647 HSQC8B6 3 727 HSQC8B6 3 1301 2 HSQC8B6 4 160 HSQC8B6 4 281 HSQC8B6 4 1067 HSQC8B6 4 1300 64 HSQC8B6 5 198 HSQC8B6 5 348 HSQC8B6 5 359 HSQC8B6 5 374 HSQC8B6 5 527 HSQC8B6 5 670 HSQC8B6 5 693 HSQC8B6 5 855 HSQC8B6 5 869 HSQC8B6 5 1570 HSQC8B6 5 1923 46 HSNCAMX1 1 184 HSNCAMX1 1 501 HSNCAMX1 1 635 HSNCAMX1 1 740 HSNCAMX1 1 763 HSNCAMX1 1 771 HSNCAMX1 1 817 HSNCAMX1 1 860 HSNCAMX1 1 876 HSNCAMX1 1 927 HSNCAMX1 1 1198 HSNCAMX1 1 1288 HSNCAMX1 1 1394 HSNCAMX1 1 2045 HSNCAMX1 1 2138 6 HSNCAMX1 2 14 HSNCAMX1 2 47 66 HSNCAMX1 7 92 2 HSNCAMX1 9 70 HSNCAMX1 10 180 HSNCAMX1 10 318 27 HSNCAMX1 11 22 2 HSNCAMX1 18 239 HSNCAMX1 18 526 HSNCAMX1 18 786 33 HSNCAMX1 19 42 HSNCAMX1 19 58 40 HSNCAMX1 25 196 9 HSNCAMX1 26 86 2 HUMREGB 2 182 88 HUMREGB 3 43 HUMREGB 3 478 46 HUMREGB 4 83 75 AF042084 2 221 AF042084 2 270 39 AF042084 3 158 64 AF042084 4 124 43 AF042084 5 41 AF042084 5 85 10 AF042084 6 290 AF042084 6 334 AF042084 6 453 73 AF042084 7 81 84 HUMHSP90B 1 249 HUMHSP90B 1 574 97 HUMHSP90B 3 23 123 HUMHSP90B 5 122 4 HUMHSP90B 6 74 24 HUMHSP90B 9 43 178 HSAPOAIA 2 364 2 HSLWBGTPT 1 29 HSLWBGTPT 1 52 66 D63861 1 91 D63861 1 490 D63861 1 601 D63861 1 918 D63861 1 1127 D63861 1 1168 D63861 1 1618 159 D63861 2 146 D63861 2 291 D63861 2 383 D63861 2 395 D63861 2 885 D63861 2 1158 D63861 2 1341 D63861 2 1976 18 D63861 3 232 D63861 3 304 D63861 3 464 D63861 3 508 D63861 3 809 D63861 3 959 D63861 3 1050 D63861 3 1383 D63861 3 1471 D63861 3 1652 D63861 3 1659 D63861 3 1754 D63861 3 1812 7 D63861 4 374 D63861 4 577 D63861 4 836 D63861 4 971 D63861 4 1007 D63861 4 1148 19 D63861 5 37 28 D63861 6 106 D63861 6 852 D63861 6 911 D63861 6 1623 2 D63861 7 310 D63861 7 444 D63861 7 579 D63861 7 621 D63861 7 666 D63861 7 761 D63861 7 781 D63861 7 841 D63861 7 868 D63861 7 1461 D63861 7 1580 D63861 7 1778 31 D63861 9 316 D63861 9 361 42 HUMRPS17A 1 3 HUMRPS17A 1 262 169 HUMRPS17A 2 685 HUMRPS17A 2 868 HUMRPS17A 2 942 2 HUMRPS17A 3 325 HUMRPS17A 3 454 31 HUMRPS17A 4 82 HUMRPS17A 4 380 HUMRPS17A 4 402 HUMRPS17A 4 502 HUMRPS17A 4 1205 82 HUMCBRG 1 136 72 HUMTHROMA 2 39 82 HUMTHROMA 3 187 HUMTHROMA 3 399 HUMTHROMA 3 1504 HUMTHROMA 3 1644 HUMTHROMA 3 1676 145 HUMG0S24B 1 169 HUMG0S24B 1 180 HUMG0S24B 1 632 HUMG0S24B 1 783 172 HUMP45C17 1 225 HUMP45C17 1 317 HUMP45C17 1 352 HUMP45C17 1 690 HUMP45C17 1 1202 HUMP45C17 1 1563 73 HUMP45C17 2 76 HUMP45C17 2 185 87 HUMP45C17 3 291 HUMP45C17 3 318 HUMP45C17 3 539 109 HUMP45C17 4 3 HUMP45C17 4 192 HUMP45C17 4 469 31 HUMP45C17 6 98 HUMP45C17 6 177 HUMP45C17 6 198 HUMP45C17 6 773 26 HUMP45C17 7 288 129 Each row includes the following information from left to right <GenBank Accession No.><Number of intron which includes the latent site/s><The coordinate of the latent site/s in the intron (in nt, counted from the 5 end of the intron)><The position of the first stop codon (in nt, counted from the 5′ end of the intron>.

Although the invention has been described in conjunction with specific embodiments thereof, it is evident that many alternatives, modifications and variations will be apparent to those skilled in the art. Accordingly, it is intended to embrace all such alternatives, modifications and variations that fall within the spirit and broad scope of the appended claims. All publications, patents and patent applications mentioned in this specification are herein incorporated in their entirety by reference into the specification, to the same extent as if each individual publication, patent or patent application was specifically and individually indicated to be incorporated herein by reference. In addition, citation or identification of any reference in this application shall not be construed as an admission that such reference is available as prior art to the present invention. 

1. A method of identifying latent splice sites, the method comprising identifying at least one intronic in-frame stop codon located upstream of a 5′ splice site sequence being a latent splice site, thereby identifying latent splice sites.
 2. A method of identifying a putative pathogenic gene, the method comprising identifying an in-frame stop codon in an intronic sequence of the gene, thereby identifying the putative pathogenic gene.
 3. A computer readable storage medium comprising data stored in a retrievable manner, said data including a plurality of genes each having an in-frame stop codon in an intron thereof.
 4. The computer readable storage medium of claim 3, wherein said data is as set forth in Table
 6. 5. A method of uncovering genes associated with a pathogenic tissue, the method comprising: (a) identifying genes having an in-frame stop codon in an intronic sequence thereof; and (b) detecting a presence or absence of a truncated expression product resultant of said in-frame stop codon in a gene of the genes which is expressed in the pathogenic tissue, thereby uncovering genes associated with the pathogenic tissue.
 6. The method of claim 5, wherein said truncated expression product is an mRNA and whereas said detecting is effected using an oligonucleotide probe.
 7. The method of claim 5, wherein said truncated expression product is a polypeptide and whereas said detecting is effected using an antibody probe.
 8. An oligonucleotide useful for detecting abnormally spliced nucleic acid sequences, the oligonucleotide comprising a nucleic acid sequence specifically hybridizable with a polynucleotide sequence including at least one in-frame stop codon located in an intronic sequence of a gene.
 9. The oligonucleotide of claim 6, wherein said gene is selected from the group consisting of the genes set forth in Table
 6. 10. A kit useful for detecting abnormally spliced nucleic acid sequences, the kit comprising at least one oligonucleotide including a nucleic acid sequence specifically hybridizable with a polynucleotide sequence including at least one in-frame stop codon located in an intronic sequence of a gene and reagents for detecting said at least one oligonucleotide when hybridized to said polynucleotide sequence.
 11. The kit of claim 10, wherein said at least one oligonucleotide is labeled.
 12. The kit of claim 10, wherein said at least one oligonucleotide is attached to a solid substrate.
 13. The kit of claim 12, wherein said solid substrate is configured as a microarray and whereas said at least one oligonucleotide includes a plurality of oligonucleotides each being attached to said microarray in a regio-specific manner.
 14. The kit of claim 10, wherein said gene is selected from the group consisting of the genes set forth in Table
 6. 15. A method of determining association between a genetic marker and a pathology, the method comprising: (a) identifying a gene having an in-frame stop codon in an intronic sequence thereof; (b) generating a probe capable of specifically hybridizing with a truncated expression product of said gene resultant from said in-frame stop codon; (c) contacting normal and pathological biological samples with said probe; and (d) detecting a level of probe binding in said normal and said pathological biological samples, to thereby determine association between a gene and a pathology.
 16. The method of claim 15, wherein said expression product is an mRNA transcript and whereas said probe is an oligonucleotide probe.
 17. The method of claim 15, wherein said expression product is a polypeptide and whereas said probe is an antibody probe.
 18. A method of detecting a presence or absence of an abnormal cellular phenotype associated with a defective transcription machinery, the method comprising: (a) expressing within a cell a recombinant polynucleotide capable of transcribing at least two distinct mRNA transcripts, wherein one of said at least two distinct mRNA transcripts encodes a reporter molecule, whereas a transcript encoding said reporter molecule forms only in cells having the defective transcription machinery; and (b) detecting a presence or absence of said reporter molecule thereby detecting a presence or absence of the abnormal cellular phenotype associated with a defective transcription machinery.
 19. The method of claim 18, wherein said reporter molecule is selected from the group consisting of a fluorescer, an enzyme and an epitope tag.
 20. A recombinant polynucleotide comprising a nucleic acid sequence being capable of transcribing at least two distinct mRNA transcripts, wherein one of said at least two distinct mRNA transcripts encodes a reporter molecule, whereas a transcript encoding said reporter molecule forms only in cells having a defective transcription machinery.
 21. A nucleic acid construct encoding the recombinant polynucleotide of claim
 20. 22. The method of claim 20, wherein said reporter molecule is selected from the group consisting of a fluorescer, an enzyme and an epitope tag.
 23. A method of killing cells having abnormal cellular phenotype associated with a defective transcription machinery, the method comprising expressing within the cells a recombinant polynucleotide capable of transcribing at least two distinct mRNA transcripts, wherein one of said at least two distinct mRNA transcripts encodes a peptide toxin, whereas a transcript encoding said peptide toxin forms only in cells having the defective transcription machinery, thereby killing cells having abnormal cellular phenotype associated with the defective transcription machinery.
 24. The method of claim 18, wherein said peptide toxin is selected from the group consisting of Pseudomonas exotoxin, Diphtheria toxin, Cholera toxin, ricin, abrin, gelonin, pertussis toxin and Shigella toxin.
 25. A method of treating a genetic disorder associated with a defective transcription machinery in a subject, the method comprising administering to the subject a therapeutically effective amount of a recombinant polynucleotide capable of transcribing at least two distinct mRNA transcripts, wherein one of said at least two distinct mRNA transcripts encodes a peptide toxin, whereas a transcript encoding said peptide toxin forms only in cells having the defective transcription machinery, thereby treating the genetic disorder associated with a defective transcription machinery.
 26. The method of claim 25, wherein said peptide toxin is selected from the group consisting of Pseudomonas exotoxin, Diphtheria toxin, Cholera toxin, ricin, abrin, gelonin, pertussis toxin and Shigella toxin.
 27. A pharmaceutical composition comprising a recombinant polynucleotide capable of transcribing at least two distinct mRNA transcripts, wherein one of said at least two distinct mRNA transcripts encodes a peptide toxin, whereas a transcript encoding said peptide toxin forms only in cells having the defective transcription machinery, and a pharmaceutically acceptable carrier or diluent.
 28. The pharmaceutical composition of claim 27, wherein said peptide toxin is selected from the group consisting of Pseudomonas exotoxin, Diphtheria toxin, Cholera toxin, ricin, abrin, gelonin, pertussis toxin and Shigella toxin.
 29. A method of treating a genetic disorder associated with abnormal splicing the method comprising fixing mutations associated with premature stop codons thereby treating genetic disorders associated with defective transcription machinery.
 30. The method of claim 29, wherein said fixing is effected by gene nock-in and whereas said gene nock-in is directed at in-frame stop codons located at intronic sequences.
 31. A method of identifying agents which affect the activity of the transcription machinery, the method comprising: (a) expressing in a plurality of cells a recombinant polynucleotide capable of transcribing at least two distinct mRNA transcripts, wherein one of said at least two distinct mRNA transcripts encodes a reporter molecule, whereas a transcript encoding said reporter molecule forms only in cells having the defective transcription machinery; (b) exposing said plurality of cells expressing said recombinant polynucleotide to a plurality of agents; and (c) identifying an agent of said plurality of agents which alters expression of said reporter molecule to thereby identify agents which affect the activity of the transcription machinery.
 32. The method of claim 31, wherein said agent up-regulates expression of said reporter molecule, to thereby identify agents which damage the transcription machinery.
 33. The method of claim 31, wherein said agent down-regulates expression of said reporter molecule, to thereby identify agents which repair the transcription machinery. 